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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.

rs1084004

Current Build 152

Released October 2, 2018

Organism
Homo sapiens
Position
chr10:71362188 (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
T>C / T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.17453 (42944/246058, GnomAD)
T=0.16262 (20420/125568, TOPMED)
T=0.16983 (20612/121372, ExAC) (+ 6 more)
T=0.1556 (4806/30894, GnomAD)
T=0.1334 (1735/13006, GO-ESP)
T=0.246 (1233/5008, 1000G)
T=0.082 (366/4480, Estonian)
T=0.088 (341/3854, ALSPAC)
T=0.093 (343/3708, TWINSUK)
Clinical Significance
Reported in ClinVar
Gene : Consequence
SLC29A3 : Synonymous Variant
Publications
0 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 10 NC_000010.11:g.71362188T>C
GRCh38.p12 chr 10 NC_000010.11:g.71362188T>G
GRCh37.p13 chr 10 NC_000010.10:g.73121945T>C
GRCh37.p13 chr 10 NC_000010.10:g.73121945T>G
SLC29A3 RefSeqGene NG_017066.1:g.47936T>C
SLC29A3 RefSeqGene NG_017066.1:g.47936T>G
Gene: SLC29A3, solute carrier family 29 member 3 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
SLC29A3 transcript variant 2 NM_001174098.1:c. N/A 3 Prime UTR Variant
SLC29A3 transcript variant 1 NM_018344.5:c.1008T>C G [GGT] > G [GGC] Coding Sequence Variant
equilibrative nucleoside transporter 3 isoform a NP_060814.4:p.Gly336= G (Gly) > G (Gly) Synonymous Variant
SLC29A3 transcript variant 1 NM_018344.5:c.1008T>G G [GGT] > G [GGG] Coding Sequence Variant
equilibrative nucleoside transporter 3 isoform a NP_060814.4:p.Gly336= G (Gly) > G (Gly) Synonymous Variant
SLC29A3 transcript variant 3 NR_033413.1:n.982T>C N/A Non Coding Transcript Variant
SLC29A3 transcript variant 3 NR_033413.1:n.982T>G N/A Non Coding Transcript Variant
SLC29A3 transcript variant 4 NR_033414.1:n.755T>C N/A Non Coding Transcript Variant
SLC29A3 transcript variant 4 NR_033414.1:n.755T>G N/A Non Coding Transcript Variant
SLC29A3 transcript variant X1 XM_006717910.4:c.774T>C G [GGT] > G [GGC] Coding Sequence Variant
equilibrative nucleoside transporter 3 isoform X1 XP_006717973.1:p.Gly258= G (Gly) > G (Gly) Synonymous Variant
SLC29A3 transcript variant X1 XM_006717910.4:c.774T>G G [GGT] > G [GGG] Coding Sequence Variant
equilibrative nucleoside transporter 3 isoform X1 XP_006717973.1:p.Gly258= G (Gly) > G (Gly) Synonymous Variant
SLC29A3 transcript variant X2 XM_017016377.2:c.570T>C G [GGT] > G [GGC] Coding Sequence Variant
equilibrative nucleoside transporter 3 isoform X2 XP_016871866.1:p.Gly190= G (Gly) > G (Gly) Synonymous Variant
SLC29A3 transcript variant X2 XM_017016377.2:c.570T>G G [GGT] > G [GGG] Coding Sequence Variant
equilibrative nucleoside transporter 3 isoform X2 XP_016871866.1:p.Gly190= G (Gly) > G (Gly) Synonymous Variant
SLC29A3 transcript variant X3 XM_017016378.2:c.390T>C G [GGT] > G [GGC] Coding Sequence Variant
equilibrative nucleoside transporter 3 isoform X3 XP_016871867.1:p.Gly130= G (Gly) > G (Gly) Synonymous Variant
SLC29A3 transcript variant X3 XM_017016378.2:c.390T>G G [GGT] > G [GGG] Coding Sequence Variant
equilibrative nucleoside transporter 3 isoform X3 XP_016871867.1:p.Gly130= G (Gly) > G (Gly) Synonymous 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.

Allele: C (allele ID: 135784 )
ClinVar Accession Disease Names Clinical Significance
RCV000118375.2 not specified Likely-Benign
RCV000318573.1 Histiocytosis-lymphadenopathy plus syndrome Benign
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 246058 T=0.17453 C=0.82547
gnomAD - Exomes European Sub 133838 T=0.10040 C=0.89960
gnomAD - Exomes Asian Sub 48028 T=0.2457 C=0.7543
gnomAD - Exomes American Sub 33572 T=0.3742 C=0.6258
gnomAD - Exomes African Sub 15300 T=0.2472 C=0.7528
gnomAD - Exomes Ashkenazi Jewish Sub 9840 T=0.056 C=0.944
gnomAD - Exomes Other Sub 5480 T=0.149 C=0.851
TopMed Global Study-wide 125568 T=0.16262 C=0.83738
ExAC Global Study-wide 121372 T=0.16983 C=0.83017
ExAC Europe Sub 73350 T=0.0980 C=0.9020
ExAC Asian Sub 25140 T=0.2442 C=0.7558
ExAC American Sub 11574 T=0.3989 C=0.6011
ExAC African Sub 10400 T=0.2433 C=0.7567
ExAC Other Sub 908 T=0.16 C=0.84
gnomAD - Genomes Global Study-wide 30894 T=0.1556 C=0.8444
gnomAD - Genomes European Sub 18462 T=0.0969 C=0.9031
gnomAD - Genomes African Sub 8698 T=0.247 C=0.753
gnomAD - Genomes East Asian Sub 1616 T=0.273 C=0.727
gnomAD - Genomes Other Sub 980 T=0.14 C=0.86
gnomAD - Genomes American Sub 836 T=0.32 C=0.68
gnomAD - Genomes Ashkenazi Jewish Sub 302 T=0.07 C=0.93
GO Exome Sequencing Project Global Study-wide 13006 T=0.1334 C=0.8666
GO Exome Sequencing Project European American Sub 8600 T=0.082 C=0.918
GO Exome Sequencing Project African American Sub 4406 T=0.233 C=0.767
1000Genomes Global Study-wide 5008 T=0.246 C=0.754
1000Genomes African Sub 1322 T=0.253 C=0.747
1000Genomes East Asian Sub 1008 T=0.285 C=0.715
1000Genomes Europe Sub 1006 T=0.102 C=0.898
1000Genomes South Asian Sub 978 T=0.28 C=0.72
1000Genomes American Sub 694 T=0.34 C=0.66
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.082 C=0.918
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.088 C=0.912
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.093 C=0.907
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 T= C G Note
GRCh38.p12 chr 10 NC_000010.11:g.71...

NC_000010.11:g.71362188T=

NC_000010.11:g.71...

NC_000010.11:g.71362188T>C

NC_000010.11:g.71...

NC_000010.11:g.71362188T>G

GRCh37.p13 chr 10 NC_000010.10:g.73...

NC_000010.10:g.73121945T=

NC_000010.10:g.73...

NC_000010.10:g.73121945T>C

NC_000010.10:g.73...

NC_000010.10:g.73121945T>G

SLC29A3 RefSeqGene NG_017066.1:g.479...

NG_017066.1:g.47936T=

NG_017066.1:g.479...

NG_017066.1:g.47936T>C

NG_017066.1:g.479...

NG_017066.1:g.47936T>G

SLC29A3 transcript variant 1 NM_018344.5:c.1008T= NM_018344.5:c.100...

NM_018344.5:c.1008T>C

NM_018344.5:c.100...

NM_018344.5:c.1008T>G

SLC29A3 transcript variant 2 NM_001174098.1:c....

NM_001174098.1:c.*237T=

NM_001174098.1:c....

NM_001174098.1:c.*237T>C

NM_001174098.1:c....

NM_001174098.1:c.*237T>G

SLC29A3 transcript variant 3 NR_033413.1:n.982T= NR_033413.1:n.982T>C NR_033413.1:n.982T>G
SLC29A3 transcript variant 4 NR_033414.1:n.755T= NR_033414.1:n.755T>C NR_033414.1:n.755T>G
SLC29A3 transcript variant X1 XM_006717910.4:c....

XM_006717910.4:c.774T=

XM_006717910.4:c....

XM_006717910.4:c.774T>C

XM_006717910.4:c....

XM_006717910.4:c.774T>G

SLC29A3 transcript variant X2 XM_017016377.2:c....

XM_017016377.2:c.570T=

XM_017016377.2:c....

XM_017016377.2:c.570T>C

XM_017016377.2:c....

XM_017016377.2:c.570T>G

SLC29A3 transcript variant X3 XM_017016378.2:c....

XM_017016378.2:c.390T=

XM_017016378.2:c....

XM_017016378.2:c.390T>C

XM_017016378.2:c....

XM_017016378.2:c.390T>G

equilibrative nucleoside transporter 3 isoform a NP_060814.4:p.Gly...

NP_060814.4:p.Gly336=

NP_060814.4:p.Gly...

NP_060814.4:p.Gly336=

NP_060814.4:p.Gly...

NP_060814.4:p.Gly336=

equilibrative nucleoside transporter 3 isoform X1 XP_006717973.1:p....

XP_006717973.1:p.Gly258=

XP_006717973.1:p....

XP_006717973.1:p.Gly258=

XP_006717973.1:p....

XP_006717973.1:p.Gly258=

equilibrative nucleoside transporter 3 isoform X2 XP_016871866.1:p....

XP_016871866.1:p.Gly190=

XP_016871866.1:p....

XP_016871866.1:p.Gly190=

XP_016871866.1:p....

XP_016871866.1:p.Gly190=

equilibrative nucleoside transporter 3 isoform X3 XP_016871867.1:p....

XP_016871867.1:p.Gly130=

XP_016871867.1:p....

XP_016871867.1:p.Gly130=

XP_016871867.1:p....

XP_016871867.1:p.Gly130=

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#.

120 SubSNP, 9 Frequency, 2 ClinVar submissions
No Submitter Submission ID Date (Build)
1 KWOK ss919334 Oct 13, 2000 (86)
2 SC_JCM ss3488769 Sep 28, 2001 (100)
3 SC_JCM ss3952767 Sep 28, 2001 (100)
4 YUSUKE ss4926460 Aug 28, 2002 (108)
5 WI_SSAHASNP ss12095184 Jul 11, 2003 (116)
6 SC_SNP ss12958069 Dec 05, 2003 (119)
7 SC_SNP ss15974436 Feb 27, 2004 (120)
8 CSHL-HAPMAP ss16487162 Feb 27, 2004 (120)
9 CSHL-HAPMAP ss17395489 Feb 27, 2004 (120)
10 SSAHASNP ss20620069 Apr 05, 2004 (121)
11 PERLEGEN ss23607332 Sep 20, 2004 (123)
12 MGC_GENOME_DIFF ss28497220 Sep 24, 2004 (126)
13 MGC_GENOME_DIFF ss28511849 Sep 24, 2004 (126)
14 MGC_GENOME_DIFF ss28513638 Sep 24, 2004 (126)
15 ILLUMINA ss65745031 Oct 15, 2006 (127)
16 ILLUMINA ss66794414 Nov 30, 2006 (127)
17 ILLUMINA ss66904083 Nov 30, 2006 (127)
18 ILLUMINA ss67026908 Nov 30, 2006 (127)
19 PERLEGEN ss69083345 May 17, 2007 (127)
20 ILLUMINA ss70381528 May 17, 2007 (127)
21 ILLUMINA ss70501567 May 26, 2008 (130)
22 ILLUMINA ss71027567 May 17, 2007 (127)
23 ILLUMINA ss75847921 Dec 06, 2007 (129)
24 HGSV ss82613276 Dec 15, 2007 (130)
25 KRIBB_YJKIM ss83679567 Dec 15, 2007 (130)
26 CORNELL ss86272469 Mar 23, 2008 (129)
27 BCMHGSC_JDW ss88265054 Mar 23, 2008 (129)
28 HUMANGENOME_JCVI ss97566421 Feb 06, 2009 (130)
29 BGI ss102890881 Dec 01, 2009 (131)
30 1000GENOMES ss109555865 Jan 24, 2009 (130)
31 1000GENOMES ss113455536 Jan 25, 2009 (130)
32 ILLUMINA ss121399141 Dec 01, 2009 (131)
33 ENSEMBL ss131922483 Dec 01, 2009 (131)
34 ENSEMBL ss131945578 Dec 01, 2009 (131)
35 ILLUMINA ss152843201 Dec 01, 2009 (131)
36 ILLUMINA ss159146607 Dec 01, 2009 (131)
37 SEATTLESEQ ss159720774 Dec 01, 2009 (131)
38 ILLUMINA ss159927857 Dec 01, 2009 (131)
39 COMPLETE_GENOMICS ss168553455 Jul 04, 2010 (132)
40 ILLUMINA ss169656854 Jul 04, 2010 (132)
41 COMPLETE_GENOMICS ss170397033 Jul 04, 2010 (132)
42 ILLUMINA ss170621229 Jul 04, 2010 (132)
43 COMPLETE_GENOMICS ss174621386 Jul 04, 2010 (132)
44 BUSHMAN ss201691196 Jul 04, 2010 (132)
45 BCM-HGSC-SUB ss207104250 Jul 04, 2010 (132)
46 1000GENOMES ss224800523 Jul 14, 2010 (132)
47 1000GENOMES ss235232289 Jul 15, 2010 (132)
48 1000GENOMES ss241926947 Jul 15, 2010 (132)
49 BL ss254420213 May 09, 2011 (134)
50 GMI ss280672658 May 04, 2012 (137)
51 GMI ss286216866 Apr 25, 2013 (138)
52 PJP ss290867940 May 09, 2011 (134)
53 NHLBI-ESP ss342300435 May 09, 2011 (134)
54 ILLUMINA ss410889342 Sep 17, 2011 (135)
55 ILLUMINA ss479371308 May 04, 2012 (137)
56 ILLUMINA ss479374484 May 04, 2012 (137)
57 ILLUMINA ss479777303 Sep 08, 2015 (146)
58 ILLUMINA ss484485790 May 04, 2012 (137)
59 1000GENOMES ss490998555 May 04, 2012 (137)
60 CLINSEQ_SNP ss491627080 May 04, 2012 (137)
61 ILLUMINA ss533370900 Sep 08, 2015 (146)
62 TISHKOFF ss562042188 Apr 25, 2013 (138)
63 SSMP ss656947661 Apr 25, 2013 (138)
64 ILLUMINA ss782689435 Sep 08, 2015 (146)
65 ILLUMINA ss825351082 Jul 19, 2016 (147)
66 ILLUMINA ss831940376 Sep 08, 2015 (146)
67 JMKIDD_LAB ss974474996 Aug 21, 2014 (142)
68 EVA-GONL ss987632677 Aug 21, 2014 (142)
69 PMT ss1040223305 Aug 21, 2014 (142)
70 JMKIDD_LAB ss1067513597 Aug 21, 2014 (142)
71 JMKIDD_LAB ss1077095150 Aug 21, 2014 (142)
72 1000GENOMES ss1337974246 Aug 21, 2014 (142)
73 DDI ss1426364218 Apr 01, 2015 (144)
74 CLINVAR ss1457615347 Nov 23, 2014 (142)
75 EVA_GENOME_DK ss1575204606 Apr 01, 2015 (144)
76 EVA_FINRISK ss1584068571 Apr 01, 2015 (144)
77 EVA_DECODE ss1597304548 Apr 01, 2015 (144)
78 EVA_UK10K_ALSPAC ss1624851271 Apr 01, 2015 (144)
79 EVA_UK10K_TWINSUK ss1667845304 Apr 01, 2015 (144)
80 EVA_EXAC ss1689942665 Apr 01, 2015 (144)
81 EVA_MGP ss1711260422 Apr 01, 2015 (144)
82 EVA_SVP ss1713190098 Apr 01, 2015 (144)
83 ILLUMINA ss1751979205 Sep 08, 2015 (146)
84 HAMMER_LAB ss1806452084 Sep 08, 2015 (146)
85 WEILL_CORNELL_DGM ss1930998019 Feb 12, 2016 (147)
86 GENOMED ss1967163024 Jul 19, 2016 (147)
87 JJLAB ss2026226699 Sep 14, 2016 (149)
88 USC_VALOUEV ss2154500875 Dec 20, 2016 (150)
89 HUMAN_LONGEVITY ss2175847125 Dec 20, 2016 (150)
90 TOPMED ss2338887251 Dec 20, 2016 (150)
91 SYSTEMSBIOZJU ss2627583469 Nov 08, 2017 (151)
92 ILLUMINA ss2632728113 Nov 08, 2017 (151)
93 GRF ss2698745520 Nov 08, 2017 (151)
94 GNOMAD ss2738311012 Nov 08, 2017 (151)
95 GNOMAD ss2748408553 Nov 08, 2017 (151)
96 GNOMAD ss2890281459 Nov 08, 2017 (151)
97 AFFY ss2985560357 Nov 08, 2017 (151)
98 SWEGEN ss3006699476 Nov 08, 2017 (151)
99 ILLUMINA ss3021251212 Nov 08, 2017 (151)
100 BIOINF_KMB_FNS_UNIBA ss3026905093 Nov 08, 2017 (151)
101 TOPMED ss3123282432 Nov 08, 2017 (151)
102 TOPMED ss3123282433 Nov 08, 2017 (151)
103 CSHL ss3349189150 Nov 08, 2017 (151)
104 ILLUMINA ss3626475009 Oct 12, 2018 (152)
105 ILLUMINA ss3632954201 Oct 12, 2018 (152)
106 ILLUMINA ss3633651574 Oct 12, 2018 (152)
107 ILLUMINA ss3634409762 Oct 12, 2018 (152)
108 ILLUMINA ss3635343980 Oct 12, 2018 (152)
109 ILLUMINA ss3636093350 Oct 12, 2018 (152)
110 ILLUMINA ss3637094662 Oct 12, 2018 (152)
111 ILLUMINA ss3637857452 Oct 12, 2018 (152)
112 ILLUMINA ss3638944949 Oct 12, 2018 (152)
113 ILLUMINA ss3639472269 Oct 12, 2018 (152)
114 ILLUMINA ss3640117104 Oct 12, 2018 (152)
115 ILLUMINA ss3641002715 Oct 12, 2018 (152)
116 ILLUMINA ss3641297009 Oct 12, 2018 (152)
117 ILLUMINA ss3642860410 Oct 12, 2018 (152)
118 OMUKHERJEE_ADBS ss3646411060 Oct 12, 2018 (152)
119 URBANLAB ss3649405530 Oct 12, 2018 (152)
120 ILLUMINA ss3651607372 Oct 12, 2018 (152)
121 1000Genomes NC_000010.10 - 73121945 Oct 12, 2018 (152)
122 The Avon Longitudinal Study of Parents and Children NC_000010.10 - 73121945 Oct 12, 2018 (152)
123 Genetic variation in the Estonian population NC_000010.10 - 73121945 Oct 12, 2018 (152)
124 ExAC NC_000010.10 - 73121945 Oct 12, 2018 (152)
125 gnomAD - Genomes NC_000010.10 - 73121945 Oct 12, 2018 (152)
126 gnomAD - Exomes NC_000010.10 - 73121945 Oct 12, 2018 (152)
127 GO Exome Sequencing Project NC_000010.10 - 73121945 Oct 12, 2018 (152)
128 TopMed NC_000010.11 - 71362188 Oct 12, 2018 (152)
129 UK 10K study - Twins NC_000010.10 - 73121945 Oct 12, 2018 (152)
130 ClinVar RCV000118375.2 Oct 12, 2018 (152)
131 ClinVar RCV000318573.1 Oct 12, 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)
rs3740457 Oct 09, 2002 (108)
rs17844835 Mar 11, 2006 (126)
rs17857547 Mar 11, 2006 (126)
rs17859336 Mar 11, 2006 (126)
rs61046410 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission ids Observation SPDI Canonical SPDI Source RSIDs
ss82613276, ss3638944949, ss3639472269 NC_000010.8:72791950:T:C NC_000010.11:71362187:T:C (self)
ss88265054, ss109555865, ss113455536, ss168553455, ss170397033, ss174621386, ss201691196, ss207104250, ss254420213, ss280672658, ss286216866, ss290867940, ss479371308, ss491627080, ss825351082, ss1597304548, ss1713190098, ss3642860410 NC_000010.9:72791950:T:C NC_000010.11:71362187:T:C (self)
50382282, 27967095, 19854240, 166742, 23982980, 5944921, 984429, 27967095, ss224800523, ss235232289, ss241926947, ss342300435, ss479374484, ss479777303, ss484485790, ss490998555, ss533370900, ss562042188, ss656947661, ss782689435, ss831940376, ss974474996, ss987632677, ss1040223305, ss1067513597, ss1077095150, ss1337974246, ss1426364218, ss1575204606, ss1584068571, ss1624851271, ss1667845304, ss1689942665, ss1711260422, ss1751979205, ss1806452084, ss1930998019, ss1967163024, ss2026226699, ss2154500875, ss2338887251, ss2627583469, ss2632728113, ss2698745520, ss2738311012, ss2748408553, ss2890281459, ss2985560357, ss3006699476, ss3021251212, ss3349189150, ss3626475009, ss3632954201, ss3633651574, ss3634409762, ss3635343980, ss3636093350, ss3637094662, ss3637857452, ss3640117104, ss3641002715, ss3641297009, ss3646411060, ss3651607372 NC_000010.10:73121944:T:C NC_000010.11:71362187:T:C (self)
RCV000118375.2, RCV000318573.1, 45592191, ss1457615347, ss2175847125, ss3026905093, ss3123282432, ss3649405530 NC_000010.11:71362187:T:C NC_000010.11:71362187:T:C (self)
ss12095184, ss12958069 NT_008583.15:21673116:T:C NC_000010.11:71362187:T:C (self)
ss15974436, ss16487162, ss17395489, ss20620069 NT_008583.16:21673099:T:C NC_000010.11:71362187:T:C (self)
ss919334, ss3488769, ss3952767, ss4926460, ss23607332, ss28497220, ss28511849, ss28513638, ss65745031, ss66794414, ss66904083, ss67026908, ss69083345, ss70381528, ss70501567, ss71027567, ss75847921, ss83679567, ss86272469, ss97566421, ss102890881, ss121399141, ss131922483, ss131945578, ss152843201, ss159146607, ss159720774, ss159927857, ss169656854, ss170621229, ss410889342 NT_030059.13:23926408:T:C NC_000010.11:71362187:T:C (self)
ss3123282433 NC_000010.11:71362187:T:G NC_000010.11:71362187:T:G (self)
Help

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

No publications for rs1084004

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.post104+4a6ee9c