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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

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.

rs6563701

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr13:39381317 (GRCh38.p14) 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
G=0.147131 (38944/264690, TOPMED)
G=0.151997 (33160/218162, ALFA)
G=0.143870 (20166/140168, GnomAD) (+ 21 more)
G=0.23041 (6511/28258, 14KJPN)
G=0.23347 (3913/16760, 8.3KJPN)
G=0.1407 (901/6404, 1000G_30x)
G=0.1444 (723/5008, 1000G)
G=0.1270 (569/4480, Estonian)
G=0.1487 (573/3854, ALSPAC)
G=0.1489 (552/3708, TWINSUK)
G=0.2601 (762/2930, KOREAN)
G=0.1737 (362/2084, HGDP_Stanford)
G=0.1691 (320/1892, HapMap)
G=0.2560 (469/1832, Korea1K)
G=0.1391 (158/1136, Daghestan)
G=0.165 (165/998, GoNL)
G=0.102 (64/626, Chileans)
G=0.125 (75/600, NorthernSweden)
G=0.194 (42/216, Qatari)
G=0.199 (43/216, Vietnamese)
A=0.454 (79/174, SGDP_PRJ)
G=0.38 (26/68, Ancient Sardinia)
G=0.23 (9/40, GENOME_DK)
A=0.45 (9/20, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LHFPL6 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 218256 A=0.847972 G=0.152028
European Sub 184310 A=0.842884 G=0.157116
African Sub 10410 A=0.85735 G=0.14265
African Others Sub 360 A=0.881 G=0.119
African American Sub 10050 A=0.85652 G=0.14348
Asian Sub 752 A=0.717 G=0.283
East Asian Sub 574 A=0.728 G=0.272
Other Asian Sub 178 A=0.680 G=0.320
Latin American 1 Sub 990 A=0.840 G=0.160
Latin American 2 Sub 9070 A=0.9158 G=0.0842
South Asian Sub 5056 A=0.9049 G=0.0951
Other Sub 7668 A=0.8537 G=0.1463


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
TopMed Global Study-wide 264690 A=0.852869 G=0.147131
Allele Frequency Aggregator Total Global 218162 A=0.848003 G=0.151997
Allele Frequency Aggregator European Sub 184234 A=0.842917 G=0.157083
Allele Frequency Aggregator African Sub 10410 A=0.85735 G=0.14265
Allele Frequency Aggregator Latin American 2 Sub 9070 A=0.9158 G=0.0842
Allele Frequency Aggregator Other Sub 7650 A=0.8537 G=0.1463
Allele Frequency Aggregator South Asian Sub 5056 A=0.9049 G=0.0951
Allele Frequency Aggregator Latin American 1 Sub 990 A=0.840 G=0.160
Allele Frequency Aggregator Asian Sub 752 A=0.717 G=0.283
gnomAD - Genomes Global Study-wide 140168 A=0.856130 G=0.143870
gnomAD - Genomes European Sub 75918 A=0.85760 G=0.14240
gnomAD - Genomes African Sub 42000 A=0.85729 G=0.14271
gnomAD - Genomes American Sub 13644 A=0.88339 G=0.11661
gnomAD - Genomes Ashkenazi Jewish Sub 3324 A=0.8117 G=0.1883
gnomAD - Genomes East Asian Sub 3128 A=0.7311 G=0.2689
gnomAD - Genomes Other Sub 2154 A=0.8593 G=0.1407
14KJPN JAPANESE Study-wide 28258 A=0.76959 G=0.23041
8.3KJPN JAPANESE Study-wide 16760 A=0.76653 G=0.23347
1000Genomes_30x Global Study-wide 6404 A=0.8593 G=0.1407
1000Genomes_30x African Sub 1786 A=0.8550 G=0.1450
1000Genomes_30x Europe Sub 1266 A=0.8531 G=0.1469
1000Genomes_30x South Asian Sub 1202 A=0.9160 G=0.0840
1000Genomes_30x East Asian Sub 1170 A=0.7684 G=0.2316
1000Genomes_30x American Sub 980 A=0.914 G=0.086
1000Genomes Global Study-wide 5008 A=0.8556 G=0.1444
1000Genomes African Sub 1322 A=0.8540 G=0.1460
1000Genomes East Asian Sub 1008 A=0.7738 G=0.2262
1000Genomes Europe Sub 1006 A=0.8479 G=0.1521
1000Genomes South Asian Sub 978 A=0.910 G=0.090
1000Genomes American Sub 694 A=0.912 G=0.088
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.8730 G=0.1270
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.8513 G=0.1487
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.8511 G=0.1489
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.7399 G=0.2601
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 A=0.8263 G=0.1737
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.747 G=0.253
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.896 G=0.104
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.791 G=0.209
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.756 G=0.244
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.847 G=0.153
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.995 G=0.005
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.85 G=0.15
HapMap Global Study-wide 1892 A=0.8309 G=0.1691
HapMap American Sub 770 A=0.849 G=0.151
HapMap African Sub 692 A=0.841 G=0.159
HapMap Asian Sub 254 A=0.783 G=0.217
HapMap Europe Sub 176 A=0.778 G=0.222
Korean Genome Project KOREAN Study-wide 1832 A=0.7440 G=0.2560
Genome-wide autozygosity in Daghestan Global Study-wide 1136 A=0.8609 G=0.1391
Genome-wide autozygosity in Daghestan Daghestan Sub 628 A=0.863 G=0.137
Genome-wide autozygosity in Daghestan Near_East Sub 144 A=0.854 G=0.146
Genome-wide autozygosity in Daghestan Central Asia Sub 122 A=0.803 G=0.197
Genome-wide autozygosity in Daghestan Europe Sub 108 A=0.833 G=0.167
Genome-wide autozygosity in Daghestan South Asian Sub 98 A=0.93 G=0.07
Genome-wide autozygosity in Daghestan Caucasus Sub 36 A=0.94 G=0.06
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.835 G=0.165
Chileans Chilean Study-wide 626 A=0.898 G=0.102
Northern Sweden ACPOP Study-wide 600 A=0.875 G=0.125
Qatari Global Study-wide 216 A=0.806 G=0.194
A Vietnamese Genetic Variation Database Global Study-wide 216 A=0.801 G=0.199
SGDP_PRJ Global Study-wide 174 A=0.454 G=0.546
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 68 A=0.62 G=0.38
The Danish reference pan genome Danish Study-wide 40 A=0.78 G=0.23
Siberian Global Study-wide 20 A=0.45 G=0.55
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.p14 chr 13 NC_000013.11:g.39381317A>G
GRCh37.p13 chr 13 NC_000013.10:g.39955454A>G
Gene: LHFPL6, LHFPL tetraspan subfamily member 6 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
LHFPL6 transcript NM_005780.3:c.386-2791T>C N/A Intron Variant
LHFPL6 transcript variant X1 XM_011534861.2:c.386-2791…

XM_011534861.2:c.386-2791T>C

 		N/A Intron 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

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
GRCh38.p14 chr 13 NC_000013.11:g.39381317= NC_000013.11:g.39381317A>G
GRCh37.p13 chr 13 NC_000013.10:g.39955454= NC_000013.10:g.39955454A>G
LHFPL6 transcript NM_005780.2:c.386-2791= NM_005780.2:c.386-2791T>C
LHFPL6 transcript NM_005780.3:c.386-2791= NM_005780.3:c.386-2791T>C
LHFPL6 transcript variant X1 XM_011534861.2:c.386-2791= XM_011534861.2:c.386-2791T>C
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#.

122 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss11095634 Jul 11, 2003 (116)
2 WI_SSAHASNP ss12265093 Jul 11, 2003 (116)
3 PERLEGEN ss14881368 Dec 05, 2003 (119)
4 PERLEGEN ss24055180 Sep 20, 2004 (123)
5 AFFY ss65933723 Nov 29, 2006 (127)
6 AFFY ss66149640 Nov 29, 2006 (127)
7 ILLUMINA ss66623020 Nov 29, 2006 (127)
8 ILLUMINA ss67472615 Nov 29, 2006 (127)
9 ILLUMINA ss67827979 Nov 29, 2006 (127)
10 PERLEGEN ss69132139 May 16, 2007 (127)
11 ILLUMINA ss70873473 May 26, 2008 (130)
12 ILLUMINA ss71462758 May 16, 2007 (127)
13 ILLUMINA ss75435804 Dec 06, 2007 (129)
14 AFFY ss76177157 Dec 06, 2007 (129)
15 ILLUMINA ss79226093 Dec 16, 2007 (130)
16 KRIBB_YJKIM ss84504826 Dec 16, 2007 (130)
17 BCMHGSC_JDW ss89614014 Mar 24, 2008 (129)
18 ILLUMINA ss122571931 Dec 01, 2009 (131)
19 ENSEMBL ss133549314 Dec 01, 2009 (131)
20 ILLUMINA ss154368767 Dec 01, 2009 (131)
21 GMI ss154697346 Dec 01, 2009 (131)
22 ILLUMINA ss159544872 Dec 01, 2009 (131)
23 ILLUMINA ss160787392 Dec 01, 2009 (131)
24 ILLUMINA ss172151498 Jul 04, 2010 (132)
25 AFFY ss172720155 Jul 04, 2010 (132)
26 ILLUMINA ss174036002 Jul 04, 2010 (132)
27 BCM-HGSC-SUB ss208496983 Jul 04, 2010 (132)
28 1000GENOMES ss211393218 Jul 14, 2010 (132)
29 1000GENOMES ss226145230 Jul 14, 2010 (132)
30 1000GENOMES ss236223367 Jul 15, 2010 (132)
31 1000GENOMES ss242724048 Jul 15, 2010 (132)
32 BL ss254949473 May 09, 2011 (134)
33 GMI ss281684477 May 04, 2012 (137)
34 PJP ss291582869 May 09, 2011 (134)
35 ILLUMINA ss481284604 May 04, 2012 (137)
36 ILLUMINA ss481309373 May 04, 2012 (137)
37 ILLUMINA ss482292139 Sep 08, 2015 (146)
38 ILLUMINA ss485437563 May 04, 2012 (137)
39 ILLUMINA ss537365179 Sep 08, 2015 (146)
40 TISHKOFF ss563622088 Apr 25, 2013 (138)
41 SSMP ss659221061 Apr 25, 2013 (138)
42 ILLUMINA ss778572823 Aug 21, 2014 (142)
43 ILLUMINA ss783164241 Aug 21, 2014 (142)
44 ILLUMINA ss784119940 Aug 21, 2014 (142)
45 ILLUMINA ss825556611 Jul 19, 2016 (147)
46 ILLUMINA ss832423666 Apr 01, 2015 (144)
47 ILLUMINA ss833056070 Aug 21, 2014 (142)
48 ILLUMINA ss833646898 Aug 21, 2014 (142)
49 ILLUMINA ss834029860 Aug 21, 2014 (142)
50 EVA-GONL ss990312292 Aug 21, 2014 (142)
51 JMKIDD_LAB ss1079026751 Aug 21, 2014 (142)
52 1000GENOMES ss1347925514 Aug 21, 2014 (142)
53 HAMMER_LAB ss1397655741 Sep 08, 2015 (146)
54 DDI ss1427165873 Apr 01, 2015 (144)
55 EVA_GENOME_DK ss1576743202 Apr 01, 2015 (144)
56 EVA_UK10K_ALSPAC ss1630122894 Apr 01, 2015 (144)
57 EVA_UK10K_TWINSUK ss1673116927 Apr 01, 2015 (144)
58 EVA_DECODE ss1684832538 Apr 01, 2015 (144)
59 EVA_SVP ss1713385312 Apr 01, 2015 (144)
60 ILLUMINA ss1752103509 Sep 08, 2015 (146)
61 HAMMER_LAB ss1807577781 Sep 08, 2015 (146)
62 WEILL_CORNELL_DGM ss1933680566 Feb 12, 2016 (147)
63 GENOMED ss1967764582 Jul 19, 2016 (147)
64 JJLAB ss2027598954 Sep 14, 2016 (149)
65 USC_VALOUEV ss2155963564 Dec 20, 2016 (150)
66 HUMAN_LONGEVITY ss2195730221 Dec 20, 2016 (150)
67 SYSTEMSBIOZJU ss2628288746 Nov 08, 2017 (151)
68 ILLUMINA ss2633054652 Nov 08, 2017 (151)
69 GRF ss2700338109 Nov 08, 2017 (151)
70 GNOMAD ss2918800943 Nov 08, 2017 (151)
71 AFFY ss2985002037 Nov 08, 2017 (151)
72 AFFY ss2985637269 Nov 08, 2017 (151)
73 SWEGEN ss3010898241 Nov 08, 2017 (151)
74 BIOINF_KMB_FNS_UNIBA ss3027616157 Nov 08, 2017 (151)
75 CSHL ss3350419962 Nov 08, 2017 (151)
76 ILLUMINA ss3627048408 Oct 12, 2018 (152)
77 ILLUMINA ss3631058427 Oct 12, 2018 (152)
78 ILLUMINA ss3633047435 Oct 12, 2018 (152)
79 ILLUMINA ss3633749682 Oct 12, 2018 (152)
80 ILLUMINA ss3634541488 Oct 12, 2018 (152)
81 ILLUMINA ss3635439818 Oct 12, 2018 (152)
82 ILLUMINA ss3636228194 Oct 12, 2018 (152)
83 ILLUMINA ss3637190890 Oct 12, 2018 (152)
84 ILLUMINA ss3638007019 Oct 12, 2018 (152)
85 ILLUMINA ss3639016458 Oct 12, 2018 (152)
86 ILLUMINA ss3639511564 Oct 12, 2018 (152)
87 ILLUMINA ss3640248819 Oct 12, 2018 (152)
88 ILLUMINA ss3641040488 Oct 12, 2018 (152)
89 ILLUMINA ss3641335377 Oct 12, 2018 (152)
90 ILLUMINA ss3642997123 Oct 12, 2018 (152)
91 ILLUMINA ss3653772732 Oct 12, 2018 (152)
92 EGCUT_WGS ss3678162963 Jul 13, 2019 (153)
93 EVA_DECODE ss3695143041 Jul 13, 2019 (153)
94 ACPOP ss3739681817 Jul 13, 2019 (153)
95 ILLUMINA ss3744842194 Jul 13, 2019 (153)
96 EVA ss3751371657 Jul 13, 2019 (153)
97 ILLUMINA ss3772341274 Jul 13, 2019 (153)
98 KHV_HUMAN_GENOMES ss3816703343 Jul 13, 2019 (153)
99 EVA ss3833507900 Apr 27, 2020 (154)
100 EVA ss3840333881 Apr 27, 2020 (154)
101 EVA ss3845819209 Apr 27, 2020 (154)
102 HGDP ss3847476237 Apr 27, 2020 (154)
103 SGDP_PRJ ss3879819773 Apr 27, 2020 (154)
104 KRGDB ss3928654635 Apr 27, 2020 (154)
105 KOGIC ss3973413859 Apr 27, 2020 (154)
106 EVA ss3985636118 Apr 26, 2021 (155)
107 EVA ss4017629102 Apr 26, 2021 (155)
108 TOPMED ss4943668341 Apr 26, 2021 (155)
109 TOMMO_GENOMICS ss5209655714 Apr 26, 2021 (155)
110 1000G_HIGH_COVERAGE ss5293473221 Oct 16, 2022 (156)
111 EVA ss5315678076 Oct 16, 2022 (156)
112 EVA ss5410295386 Oct 16, 2022 (156)
113 HUGCELL_USP ss5487864470 Oct 16, 2022 (156)
114 1000G_HIGH_COVERAGE ss5592293555 Oct 16, 2022 (156)
115 SANFORD_IMAGENETICS ss5654620524 Oct 16, 2022 (156)
116 TOMMO_GENOMICS ss5761433180 Oct 16, 2022 (156)
117 EVA ss5799895253 Oct 16, 2022 (156)
118 YY_MCH ss5814045120 Oct 16, 2022 (156)
119 EVA ss5839373010 Oct 16, 2022 (156)
120 EVA ss5850695699 Oct 16, 2022 (156)
121 EVA ss5924808156 Oct 16, 2022 (156)
122 EVA ss5946035286 Oct 16, 2022 (156)
123 1000Genomes NC_000013.10 - 39955454 Oct 12, 2018 (152)
124 1000Genomes_30x NC_000013.11 - 39381317 Oct 16, 2022 (156)
125 The Avon Longitudinal Study of Parents and Children NC_000013.10 - 39955454 Oct 12, 2018 (152)
126 Chileans NC_000013.10 - 39955454 Apr 27, 2020 (154)
127 Genome-wide autozygosity in Daghestan NC_000013.9 - 38853454 Apr 27, 2020 (154)
128 Genetic variation in the Estonian population NC_000013.10 - 39955454 Oct 12, 2018 (152)
129 The Danish reference pan genome NC_000013.10 - 39955454 Apr 27, 2020 (154)
130 gnomAD - Genomes NC_000013.11 - 39381317 Apr 26, 2021 (155)
131 Genome of the Netherlands Release 5 NC_000013.10 - 39955454 Apr 27, 2020 (154)
132 HGDP-CEPH-db Supplement 1 NC_000013.9 - 38853454 Apr 27, 2020 (154)
133 HapMap NC_000013.11 - 39381317 Apr 27, 2020 (154)
134 KOREAN population from KRGDB NC_000013.10 - 39955454 Apr 27, 2020 (154)
135 Korean Genome Project NC_000013.11 - 39381317 Apr 27, 2020 (154)
136 Northern Sweden NC_000013.10 - 39955454 Jul 13, 2019 (153)
137 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000013.10 - 39955454 Apr 26, 2021 (155)
138 Qatari NC_000013.10 - 39955454 Apr 27, 2020 (154)
139 SGDP_PRJ NC_000013.10 - 39955454 Apr 27, 2020 (154)
140 Siberian NC_000013.10 - 39955454 Apr 27, 2020 (154)
141 8.3KJPN NC_000013.10 - 39955454 Apr 26, 2021 (155)
142 14KJPN NC_000013.11 - 39381317 Oct 16, 2022 (156)
143 TopMed NC_000013.11 - 39381317 Apr 26, 2021 (155)
144 UK 10K study - Twins NC_000013.10 - 39955454 Oct 12, 2018 (152)
145 A Vietnamese Genetic Variation Database NC_000013.10 - 39955454 Jul 13, 2019 (153)
146 ALFA NC_000013.11 - 39381317 Apr 26, 2021 (155)
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)
rs61201006 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
126389, 154129, ss89614014, ss160787392, ss208496983, ss211393218, ss254949473, ss281684477, ss291582869, ss481284604, ss825556611, ss1397655741, ss1684832538, ss1713385312, ss3639016458, ss3639511564, ss3642997123, ss3847476237 NC_000013.9:38853453:A:G NC_000013.11:39381316:A:G (self)
60785485, 33765954, 118391, 23901211, 3268730, 15066893, 35832029, 12966682, 862045, 15722496, 31836753, 8479918, 67625021, 33765954, 7490873, ss226145230, ss236223367, ss242724048, ss481309373, ss482292139, ss485437563, ss537365179, ss563622088, ss659221061, ss778572823, ss783164241, ss784119940, ss832423666, ss833056070, ss833646898, ss834029860, ss990312292, ss1079026751, ss1347925514, ss1427165873, ss1576743202, ss1630122894, ss1673116927, ss1752103509, ss1807577781, ss1933680566, ss1967764582, ss2027598954, ss2155963564, ss2628288746, ss2633054652, ss2700338109, ss2918800943, ss2985002037, ss2985637269, ss3010898241, ss3350419962, ss3627048408, ss3631058427, ss3633047435, ss3633749682, ss3634541488, ss3635439818, ss3636228194, ss3637190890, ss3638007019, ss3640248819, ss3641040488, ss3641335377, ss3653772732, ss3678162963, ss3739681817, ss3744842194, ss3751371657, ss3772341274, ss3833507900, ss3840333881, ss3879819773, ss3928654635, ss3985636118, ss4017629102, ss5209655714, ss5315678076, ss5410295386, ss5654620524, ss5799895253, ss5839373010, ss5946035286 NC_000013.10:39955453:A:G NC_000013.11:39381316:A:G (self)
79819490, 428572797, 974016, 29791860, 95270284, 159213999, 6910962902, ss2195730221, ss3027616157, ss3695143041, ss3816703343, ss3845819209, ss3973413859, ss4943668341, ss5293473221, ss5487864470, ss5592293555, ss5761433180, ss5814045120, ss5850695699, ss5924808156 NC_000013.11:39381316:A:G NC_000013.11:39381316:A:G (self)
ss11095634, ss12265093 NT_024524.12:8529944:A:G NC_000013.11:39381316:A:G (self)
ss14881368, ss24055180, ss65933723, ss66149640, ss66623020, ss67472615, ss67827979, ss69132139, ss70873473, ss71462758, ss75435804, ss76177157, ss79226093, ss84504826, ss122571931, ss133549314, ss154368767, ss154697346, ss159544872, ss172151498, ss172720155, ss174036002 NT_024524.14:20935453:A:G NC_000013.11:39381316: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.

No publications for rs6563701

Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

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.post761+d5e8e07