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dbSNP Short Genetic Variations

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs735943

Current Build 152

Released October 2, 2018

Organism
Homo sapiens
Position
chr1:241866849 (GRCh38.p12) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.40282 (99164/246172, GnomAD)
A=0.40214 (50496/125568, TOPMED)
A=0.40704 (49406/121380, ExAC) (+ 6 more)
A=0.3933 (12143/30876, GnomAD)
A=0.4326 (5626/13006, GO-ESP)
A=0.363 (1818/5008, 1000G)
A=0.380 (1704/4480, Estonian)
A=0.455 (1753/3854, ALSPAC)
A=0.439 (1627/3708, TWINSUK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
EXO1 : Missense Variant
Publications
2 citations
Genomic View
See rs on genome
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p12 chr 1 NC_000001.11:g.241866849A>G
GRCh37.p13 chr 1 NC_000001.10:g.242030151A>G
EXO1 RefSeqGene NG_029100.1:g.23659A>G
Gene: EXO1, exonuclease 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
EXO1 transcript variant 3 NM_003686.4:c.1061A>G H [CAT] > R [CGT] Coding Sequence Variant
exonuclease 1 isoform a NP_003677.4:p.His354Arg H (His) > R (Arg) Missense Variant
EXO1 transcript variant 1 NM_006027.4:c.1061A>G H [CAT] > R [CGT] Coding Sequence Variant
exonuclease 1 isoform b NP_006018.4:p.His354Arg H (His) > R (Arg) Missense Variant
EXO1 transcript variant 2 NM_130398.3:c.1061A>G H [CAT] > R [CGT] Coding Sequence Variant
exonuclease 1 isoform b NP_569082.2:p.His354Arg H (His) > R (Arg) Missense Variant
EXO1 transcript variant 4 NM_001319224.1:c.1061A>G H [CAT] > R [CGT] Coding Sequence Variant
exonuclease 1 isoform c NP_001306153.1:p.His354Arg H (His) > R (Arg) Missense Variant
EXO1 transcript variant X3 XM_011544322.1:c.1061A>G H [CAT] > R [CGT] Coding Sequence Variant
exonuclease 1 isoform X1 XP_011542624.1:p.His354Arg H (His) > R (Arg) Missense Variant
EXO1 transcript variant X1 XM_006711840.2:c.1061A>G H [CAT] > R [CGT] Coding Sequence Variant
exonuclease 1 isoform X1 XP_006711903.1:p.His354Arg H (His) > R (Arg) Missense Variant
EXO1 transcript variant X4 XM_011544323.2:c.1061A>G H [CAT] > R [CGT] Coding Sequence Variant
exonuclease 1 isoform X2 XP_011542625.1:p.His354Arg H (His) > R (Arg) Missense Variant
EXO1 transcript variant X5 XM_011544324.2:c.941A>G H [CAT] > R [CGT] Coding Sequence Variant
exonuclease 1 isoform X3 XP_011542626.1:p.His314Arg H (His) > R (Arg) Missense Variant
EXO1 transcript variant X7 XM_011544325.2:c.98A>G H [CAT] > R [CGT] Coding Sequence Variant
exonuclease 1 isoform X4 XP_011542627.1:p.His33Arg H (His) > R (Arg) Missense Variant
EXO1 transcript variant X2 XM_011544321.2:c.1061A>G H [CAT] > R [CGT] Coding Sequence Variant
exonuclease 1 isoform X1 XP_011542623.1:p.His354Arg H (His) > R (Arg) Missense Variant
EXO1 transcript variant X6 XM_017002793.2:c.941A>G H [CAT] > R [CGT] Coding Sequence Variant
exonuclease 1 isoform X3 XP_016858282.1:p.His314Arg H (His) > R (Arg) Missense Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar
Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
gnomAD - Exomes Global Study-wide 246172 A=0.40282 G=0.59718
gnomAD - Exomes European Sub 133936 A=0.43634 G=0.56366
gnomAD - Exomes Asian Sub 48030 A=0.3703 G=0.6297
gnomAD - Exomes American Sub 33572 A=0.2794 G=0.7206
gnomAD - Exomes African Sub 15304 A=0.3773 G=0.6227
gnomAD - Exomes Ashkenazi Jewish Sub 9848 A=0.558 G=0.442
gnomAD - Exomes Other Sub 5482 A=0.418 G=0.582
TopMed Global Study-wide 125568 A=0.40214 G=0.59786
gnomAD - Genomes Global Study-wide 30876 A=0.3933 G=0.6067
gnomAD - Genomes European Sub 18440 A=0.4155 G=0.5845
gnomAD - Genomes African Sub 8710 A=0.382 G=0.618
gnomAD - Genomes East Asian Sub 1612 A=0.213 G=0.787
gnomAD - Genomes Other Sub 976 A=0.41 G=0.59
gnomAD - Genomes American Sub 836 A=0.32 G=0.68
gnomAD - Genomes Ashkenazi Jewish Sub 302 A=0.48 G=0.52
GO Exome Sequencing Project Global Study-wide 13006 A=0.4326 G=0.5674
GO Exome Sequencing Project European American Sub 8600 A=0.460 G=0.540
GO Exome Sequencing Project African American Sub 4406 A=0.378 G=0.622
1000Genomes Global Study-wide 5008 A=0.363 G=0.637
1000Genomes African Sub 1322 A=0.385 G=0.615
1000Genomes East Asian Sub 1008 A=0.204 G=0.796
1000Genomes Europe Sub 1006 A=0.428 G=0.572
1000Genomes South Asian Sub 978 A=0.47 G=0.53
1000Genomes American Sub 694 A=0.31 G=0.69
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.380 G=0.620
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.455 G=0.545
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.439 G=0.561
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement A= G Note
GRCh38.p12 chr 1 NC_000001.11:g.241866849A= NC_000001.11:g.24186684...

NC_000001.11:g.241866849A>G

GRCh37.p13 chr 1 NC_000001.10:g.242030151A= NC_000001.10:g.24203015...

NC_000001.10:g.242030151A>G

EXO1 RefSeqGene NG_029100.1:g.23659A= NG_029100.1:g.23659A>G
EXO1 transcript variant 1 NM_006027.4:c.1061A= NM_006027.4:c.1061A>G
EXO1 transcript variant 3 NM_003686.4:c.1061A= NM_003686.4:c.1061A>G
EXO1 transcript variant 2 NM_130398.3:c.1061A= NM_130398.3:c.1061A>G
EXO1 transcript variant 4 NM_001319224.1:c.1061A= NM_001319224.1:c.1061A>G
EXO1 transcript variant X1 XM_006711840.2:c.1061A= XM_006711840.2:c.1061A>G
EXO1 transcript variant X4 XM_011544323.2:c.1061A= XM_011544323.2:c.1061A>G
EXO1 transcript variant X2 XM_011544321.2:c.1061A= XM_011544321.2:c.1061A>G
EXO1 transcript variant X5 XM_011544324.2:c.941A= XM_011544324.2:c.941A>G
EXO1 transcript variant X6 XM_017002793.2:c.941A= XM_017002793.2:c.941A>G
EXO1 transcript variant X7 XM_011544325.2:c.98A= XM_011544325.2:c.98A>G
EXO1 transcript variant X3 XM_011544322.1:c.1061A= XM_011544322.1:c.1061A>G
exonuclease 1 isoform b NP_006018.4:p.His354= NP_006018.4:p.His354Arg
exonuclease 1 isoform a NP_003677.4:p.His354= NP_003677.4:p.His354Arg
exonuclease 1 isoform b NP_569082.2:p.His354= NP_569082.2:p.His354Arg
exonuclease 1 isoform c NP_001306153.1:p.His354= NP_001306153.1:p.His354Arg
exonuclease 1 isoform X1 XP_006711903.1:p.His354= XP_006711903.1:p.His354Arg
exonuclease 1 isoform X2 XP_011542625.1:p.His354= XP_011542625.1:p.His354Arg
exonuclease 1 isoform X1 XP_011542623.1:p.His354= XP_011542623.1:p.His354Arg
exonuclease 1 isoform X3 XP_011542626.1:p.His314= XP_011542626.1:p.His314Arg
exonuclease 1 isoform X3 XP_016858282.1:p.His314= XP_016858282.1:p.His314Arg
exonuclease 1 isoform X4 XP_011542627.1:p.His33= XP_011542627.1:p.His33Arg
exonuclease 1 isoform X1 XP_011542624.1:p.His354= XP_011542624.1:p.His354Arg
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

139 SubSNP, 9 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss82476 Oct 05, 2000 (86)
2 SC_JCM ss2637865 Nov 08, 2000 (89)
3 EGP_SNPS ss5604802 Dec 12, 2002 (110)
4 CSHL-HAPMAP ss17341278 Feb 27, 2004 (120)
5 CSHL-HAPMAP ss19113933 Feb 27, 2004 (120)
6 PERLEGEN ss24635512 Sep 20, 2004 (123)
7 ABI ss44110363 Mar 13, 2006 (126)
8 SNP500CANCER ss48294159 Mar 13, 2006 (126)
9 APPLERA_GI ss48405189 Mar 13, 2006 (126)
10 ILLUMINA ss65729363 Oct 16, 2006 (127)
11 ILLUMINA ss66594186 Dec 01, 2006 (127)
12 ILLUMINA ss67573247 Dec 01, 2006 (127)
13 ILLUMINA ss67954228 Dec 01, 2006 (127)
14 PERLEGEN ss68799296 May 17, 2007 (127)
15 ILLUMINA ss70925240 May 25, 2008 (130)
16 ILLUMINA ss71526072 May 17, 2007 (127)
17 AFFY ss74810271 Aug 16, 2007 (128)
18 ILLUMINA ss74961696 Dec 07, 2007 (129)
19 AFFY ss76662758 Dec 07, 2007 (129)
20 SI_EXO ss76889822 Dec 07, 2007 (129)
21 ILLUMINA ss79255336 Dec 15, 2007 (130)
22 KRIBB_YJKIM ss83540866 Dec 15, 2007 (130)
23 HGSV ss83833975 Dec 15, 2007 (130)
24 HGSV ss85733083 Dec 15, 2007 (130)
25 CANCER-GENOME ss86342347 Mar 23, 2008 (129)
26 HUMANGENOME_JCVI ss99302133 Feb 05, 2009 (130)
27 BGI ss106644826 Feb 05, 2009 (130)
28 1000GENOMES ss109097992 Jan 23, 2009 (130)
29 1000GENOMES ss112048276 Jan 25, 2009 (130)
30 ILLUMINA-UK ss119273716 Feb 15, 2009 (130)
31 ILLUMINA ss122746712 Dec 01, 2009 (131)
32 ENSEMBL ss142976501 Dec 01, 2009 (131)
33 ILLUMINA ss154422214 Dec 01, 2009 (131)
34 GMI ss156509684 Dec 01, 2009 (131)
35 ILLUMINA ss159597312 Dec 01, 2009 (131)
36 SEATTLESEQ ss159701035 Dec 01, 2009 (131)
37 ILLUMINA ss160876203 Dec 01, 2009 (131)
38 COMPLETE_GENOMICS ss165552578 Jul 04, 2010 (132)
39 COMPLETE_GENOMICS ss165938684 Jul 04, 2010 (132)
40 ILLUMINA ss172285433 Jul 04, 2010 (132)
41 ILLUMINA ss174356186 Jul 04, 2010 (132)
42 BUSHMAN ss199846541 Jul 04, 2010 (132)
43 1000GENOMES ss218981988 Jul 14, 2010 (132)
44 1000GENOMES ss230977500 Jul 14, 2010 (132)
45 1000GENOMES ss238576635 Jul 15, 2010 (132)
46 ILLUMINA ss244309316 Jul 04, 2010 (132)
47 BL ss253925463 May 09, 2011 (134)
48 GMI ss276291722 May 04, 2012 (137)
49 GMI ss284261880 Apr 25, 2013 (138)
50 PJP ss290772231 May 09, 2011 (134)
51 NHLBI-ESP ss342039518 May 09, 2011 (134)
52 ILLUMINA ss481555853 May 04, 2012 (137)
53 ILLUMINA ss481585203 May 04, 2012 (137)
54 ILLUMINA ss482557623 Sep 08, 2015 (146)
55 ILLUMINA ss485572927 May 04, 2012 (137)
56 1000GENOMES ss489799458 May 04, 2012 (137)
57 EXOME_CHIP ss491313406 May 04, 2012 (137)
58 CLINSEQ_SNP ss491618730 May 04, 2012 (137)
59 ILLUMINA ss537467988 Sep 08, 2015 (146)
60 TISHKOFF ss555258156 Apr 25, 2013 (138)
61 SSMP ss648832377 Apr 25, 2013 (138)
62 ILLUMINA ss778602138 Aug 21, 2014 (142)
63 ILLUMINA ss780766280 Sep 08, 2015 (146)
64 ILLUMINA ss783232024 Sep 08, 2015 (146)
65 ILLUMINA ss783445629 Sep 08, 2015 (146)
66 ILLUMINA ss784186161 Aug 21, 2014 (142)
67 ILLUMINA ss825585854 Jul 19, 2016 (147)
68 ILLUMINA ss832492453 Sep 08, 2015 (146)
69 ILLUMINA ss834059435 Aug 21, 2014 (142)
70 JMKIDD_LAB ss974440647 Aug 21, 2014 (142)
71 EVA-GONL ss976338134 Aug 21, 2014 (142)
72 JMKIDD_LAB ss1067433997 Aug 21, 2014 (142)
73 JMKIDD_LAB ss1068748470 Aug 21, 2014 (142)
74 1000GENOMES ss1295362305 Aug 21, 2014 (142)
75 HAMMER_LAB ss1397278525 Sep 08, 2015 (146)
76 DDI ss1426169496 Apr 01, 2015 (144)
77 EVA_GENOME_DK ss1574803822 Apr 01, 2015 (144)
78 EVA_FINRISK ss1584016325 Apr 01, 2015 (144)
79 EVA_DECODE ss1585742732 Apr 01, 2015 (144)
80 EVA_UK10K_ALSPAC ss1602522554 Apr 01, 2015 (144)
81 EVA_UK10K_TWINSUK ss1645516587 Apr 01, 2015 (144)
82 EVA_EXAC ss1686140091 Apr 01, 2015 (144)
83 EVA_MGP ss1710950195 Apr 01, 2015 (144)
84 EVA_SVP ss1712420571 Apr 01, 2015 (144)
85 ILLUMINA ss1751909553 Sep 08, 2015 (146)
86 ILLUMINA ss1751909554 Sep 08, 2015 (146)
87 HAMMER_LAB ss1796007598 Sep 08, 2015 (146)
88 ILLUMINA ss1917744702 Feb 12, 2016 (147)
89 WEILL_CORNELL_DGM ss1919560013 Feb 12, 2016 (147)
90 ILLUMINA ss1946028824 Feb 12, 2016 (147)
91 ILLUMINA ss1946028825 Feb 12, 2016 (147)
92 ILLUMINA ss1958374399 Feb 12, 2016 (147)
93 ILLUMINA ss1958374400 Feb 12, 2016 (147)
94 GENOMED ss1967019935 Jul 19, 2016 (147)
95 JJLAB ss2020307874 Sep 14, 2016 (149)
96 USC_VALOUEV ss2148345826 Dec 20, 2016 (150)
97 HUMAN_LONGEVITY ss2171552185 Dec 20, 2016 (150)
98 TOPMED ss2334205062 Dec 20, 2016 (150)
99 SYSTEMSBIOZJU ss2624667317 Nov 08, 2017 (151)
100 ILLUMINA ss2632654217 Nov 08, 2017 (151)
101 ILLUMINA ss2635009144 Nov 08, 2017 (151)
102 GRF ss2698349590 Nov 08, 2017 (151)
103 ILLUMINA ss2710699180 Nov 08, 2017 (151)
104 GNOMAD ss2732406328 Nov 08, 2017 (151)
105 GNOMAD ss2746602035 Nov 08, 2017 (151)
106 GNOMAD ss2768212399 Nov 08, 2017 (151)
107 AFFY ss2984900373 Nov 08, 2017 (151)
108 AFFY ss2985544813 Nov 08, 2017 (151)
109 SWEGEN ss2988747408 Nov 08, 2017 (151)
110 ILLUMINA ss3021199023 Nov 08, 2017 (151)
111 ILLUMINA ss3021199024 Nov 08, 2017 (151)
112 EVA_SAMSUNG_MC ss3023057762 Nov 08, 2017 (151)
113 BIOINF_KMB_FNS_UNIBA ss3023916455 Nov 08, 2017 (151)
114 TOPMED ss3107960671 Nov 08, 2017 (151)
115 CSHL ss3343999602 Nov 08, 2017 (151)
116 ILLUMINA ss3625570652 Oct 11, 2018 (152)
117 ILLUMINA ss3626351975 Oct 11, 2018 (152)
118 ILLUMINA ss3626351976 Oct 11, 2018 (152)
119 ILLUMINA ss3630682869 Oct 11, 2018 (152)
120 ILLUMINA ss3632932721 Oct 11, 2018 (152)
121 ILLUMINA ss3633629100 Oct 11, 2018 (152)
122 ILLUMINA ss3634382750 Oct 11, 2018 (152)
123 ILLUMINA ss3634382751 Oct 11, 2018 (152)
124 ILLUMINA ss3635322041 Oct 11, 2018 (152)
125 ILLUMINA ss3636062029 Oct 11, 2018 (152)
126 ILLUMINA ss3637072603 Oct 11, 2018 (152)
127 ILLUMINA ss3637825247 Oct 11, 2018 (152)
128 ILLUMINA ss3638927828 Oct 11, 2018 (152)
129 ILLUMINA ss3639463037 Oct 11, 2018 (152)
130 ILLUMINA ss3640090103 Oct 11, 2018 (152)
131 ILLUMINA ss3640090104 Oct 11, 2018 (152)
132 ILLUMINA ss3642830651 Oct 11, 2018 (152)
133 ILLUMINA ss3644524836 Oct 11, 2018 (152)
134 ILLUMINA ss3644524837 Oct 11, 2018 (152)
135 OMUKHERJEE_ADBS ss3646256240 Oct 11, 2018 (152)
136 URBANLAB ss3646928327 Oct 11, 2018 (152)
137 ILLUMINA ss3651545195 Oct 11, 2018 (152)
138 ILLUMINA ss3651545196 Oct 11, 2018 (152)
139 ILLUMINA ss3653670390 Oct 11, 2018 (152)
140 1000Genomes NC_000001.10 - 242030151 Oct 11, 2018 (152)
141 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 242030151 Oct 11, 2018 (152)
142 Genetic variation in the Estonian population NC_000001.10 - 242030151 Oct 11, 2018 (152)
143 ExAC NC_000001.10 - 242030151 Oct 11, 2018 (152)
144 gnomAD - Genomes NC_000001.10 - 242030151 Oct 11, 2018 (152)
145 gnomAD - Exomes NC_000001.10 - 242030151 Oct 11, 2018 (152)
146 GO Exome Sequencing Project NC_000001.10 - 242030151 Oct 11, 2018 (152)
147 TopMed NC_000001.11 - 241866849 Oct 11, 2018 (152)
148 UK 10K study - Twins NC_000001.10 - 242030151 Oct 11, 2018 (152)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID History Updated (Build)
rs17391620 Oct 07, 2004 (123)
rs52795383 Sep 21, 2007 (128)
rs59790129 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission ids Observation SPDI Canonical SPDI Source RSIDs
ss83833975, ss85733083, ss3638927828, ss3639463037 NC_000001.8:238356191:A= NC_000001.11:241866848:A= (self)
ss109097992, ss112048276, ss119273716, ss160876203, ss165552578, ss165938684, ss199846541, ss244309316, ss253925463, ss276291722, ss284261880, ss290772231, ss481555853, ss491618730, ss825585854, ss1397278525, ss1585742732, ss1712420571, ss2635009144, ss3642830651 NC_000001.9:240096773:A= NC_000001.11:241866848:A= (self)
6243637, 3460451, 2447299, 5383244, 17611598, 1148532, 192447, 3460451, ss218981988, ss230977500, ss238576635, ss342039518, ss481585203, ss482557623, ss485572927, ss489799458, ss491313406, ss537467988, ss555258156, ss648832377, ss778602138, ss780766280, ss783232024, ss783445629, ss784186161, ss832492453, ss834059435, ss974440647, ss976338134, ss1067433997, ss1068748470, ss1295362305, ss1426169496, ss1574803822, ss1584016325, ss1602522554, ss1645516587, ss1686140091, ss1710950195, ss1751909553, ss1751909554, ss1796007598, ss1917744702, ss1919560013, ss1946028824, ss1946028825, ss1958374399, ss1958374400, ss1967019935, ss2020307874, ss2148345826, ss2334205062, ss2624667317, ss2632654217, ss2698349590, ss2710699180, ss2732406328, ss2746602035, ss2768212399, ss2984900373, ss2985544813, ss2988747408, ss3021199023, ss3021199024, ss3023057762, ss3343999602, ss3625570652, ss3626351975, ss3626351976, ss3630682869, ss3632932721, ss3633629100, ss3634382750, ss3634382751, ss3635322041, ss3636062029, ss3637072603, ss3637825247, ss3640090103, ss3640090104, ss3644524836, ss3644524837, ss3646256240, ss3651545195, ss3651545196, ss3653670390 NC_000001.10:242030150:A= NC_000001.11:241866848:A= (self)
33517553, ss2171552185, ss3023916455, ss3107960671, ss3646928327 NC_000001.11:241866848:A= NC_000001.11:241866848:A= (self)
ss17341278, ss19113933 NT_004836.15:6787939:A= NC_000001.11:241866848:A= (self)
ss76889822 NT_004836.17:6787939:A= NC_000001.11:241866848:A= (self)
ss82476, ss2637865, ss5604802, ss24635512, ss44110363, ss48294159, ss48405189, ss65729363, ss66594186, ss67573247, ss67954228, ss68799296, ss70925240, ss71526072, ss74810271, ss74961696, ss76662758, ss79255336, ss83540866, ss86342347, ss99302133, ss106644826, ss122746712, ss142976501, ss154422214, ss156509684, ss159597312, ss159701035, ss172285433, ss174356186 NT_167186.1:35547929:A= NC_000001.11:241866848:A= (self)
ss83833975, ss85733083, ss3638927828, ss3639463037 NC_000001.8:238356191:A>G NC_000001.11:241866848:A>G (self)
ss109097992, ss112048276, ss119273716, ss160876203, ss165552578, ss165938684, ss199846541, ss244309316, ss253925463, ss276291722, ss284261880, ss290772231, ss481555853, ss491618730, ss825585854, ss1397278525, ss1585742732, ss1712420571, ss2635009144, ss3642830651 NC_000001.9:240096773:A>G NC_000001.11:241866848:A>G (self)
6243637, 3460451, 2447299, 5383244, 17611598, 1148532, 192447, 3460451, ss218981988, ss230977500, ss238576635, ss342039518, ss481585203, ss482557623, ss485572927, ss489799458, ss491313406, ss537467988, ss555258156, ss648832377, ss778602138, ss780766280, ss783232024, ss783445629, ss784186161, ss832492453, ss834059435, ss974440647, ss976338134, ss1067433997, ss1068748470, ss1295362305, ss1426169496, ss1574803822, ss1584016325, ss1602522554, ss1645516587, ss1686140091, ss1710950195, ss1751909553, ss1751909554, ss1796007598, ss1917744702, ss1919560013, ss1946028824, ss1946028825, ss1958374399, ss1958374400, ss1967019935, ss2020307874, ss2148345826, ss2334205062, ss2624667317, ss2632654217, ss2698349590, ss2710699180, ss2732406328, ss2746602035, ss2768212399, ss2984900373, ss2985544813, ss2988747408, ss3021199023, ss3021199024, ss3023057762, ss3343999602, ss3625570652, ss3626351975, ss3626351976, ss3630682869, ss3632932721, ss3633629100, ss3634382750, ss3634382751, ss3635322041, ss3636062029, ss3637072603, ss3637825247, ss3640090103, ss3640090104, ss3644524836, ss3644524837, ss3646256240, ss3651545195, ss3651545196, ss3653670390 NC_000001.10:242030150:A>G NC_000001.11:241866848:A>G (self)
33517553, ss2171552185, ss3023916455, ss3107960671, ss3646928327 NC_000001.11:241866848:A>G NC_000001.11:241866848:A>G (self)
ss17341278, ss19113933 NT_004836.15:6787939:A>G NC_000001.11:241866848:A>G (self)
ss76889822 NT_004836.17:6787939:A>G NC_000001.11:241866848:A>G (self)
ss82476, ss2637865, ss5604802, ss24635512, ss44110363, ss48294159, ss48405189, ss65729363, ss66594186, ss67573247, ss67954228, ss68799296, ss70925240, ss71526072, ss74810271, ss74961696, ss76662758, ss79255336, ss83540866, ss86342347, ss99302133, ss106644826, ss122746712, ss142976501, ss154422214, ss156509684, ss159597312, ss159701035, ss172285433, ss174356186 NT_167186.1:35547929:A>G NC_000001.11:241866848:A>G (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

2 citations for rs735943
PMID Title Author Year Journal
26724419 Polymorphisms in mismatch repair genes are associated with risk and microsatellite instability of gastric cancer, and interact with life exposures. Zhu H et al. 2016 Gene
26811195 Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families. Talseth-Palmer BA et al. 2016 Cancer medicine

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post58+e54ea20