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dbSNP Short Genetic Variations

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.

rs72928978

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr11:69063896 (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
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.067691 (17917/264690, TOPMED)
A=0.094228 (23433/248684, GnomAD_exome)
A=0.110896 (23634/213118, ALFA) (+ 19 more)
A=0.091331 (12801/140160, GnomAD)
A=0.099663 (11662/117014, ExAC)
A=0.02609 (2048/78512, PAGE_STUDY)
A=0.08585 (1115/12988, GO-ESP)
A=0.0378 (242/6404, 1000G_30x)
A=0.0397 (199/5008, 1000G)
A=0.2394 (1072/4478, Estonian)
A=0.0968 (373/3854, ALSPAC)
A=0.1033 (383/3708, TWINSUK)
A=0.0003 (1/2920, KOREAN)
A=0.003 (2/614, Vietnamese)
A=0.173 (104/600, NorthernSweden)
A=0.021 (11/534, MGP)
A=0.259 (70/270, FINRISK)
A=0.023 (5/216, Qatari)
G=0.45 (26/58, SGDP_PRJ)
A=0.15 (6/40, GENOME_DK)
G=0.5 (5/10, Siberian)
A=0.5 (5/10, Siberian)
Clinical Significance
Reported in ClinVar
Gene : Consequence
TPCN2 : Missense Variant
Publications
1 citation
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 229432 G=0.890272 A=0.109728
European Sub 191618 G=0.880424 A=0.119576
African Sub 9660 G=0.9789 A=0.0211
African Others Sub 360 G=0.992 A=0.008
African American Sub 9300 G=0.9784 A=0.0216
Asian Sub 3382 G=0.9982 A=0.0018
East Asian Sub 2696 G=0.9981 A=0.0019
Other Asian Sub 686 G=0.999 A=0.001
Latin American 1 Sub 866 G=0.955 A=0.045
Latin American 2 Sub 5066 G=0.9660 A=0.0340
South Asian Sub 290 G=0.976 A=0.024
Other Sub 18550 G=0.90113 A=0.09887


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 G=0.932309 A=0.067691
gnomAD - Exomes Global Study-wide 248684 G=0.905772 A=0.094228
gnomAD - Exomes European Sub 132992 G=0.853645 A=0.146355
gnomAD - Exomes Asian Sub 48934 G=0.98220 A=0.01780
gnomAD - Exomes American Sub 34474 G=0.97134 A=0.02866
gnomAD - Exomes African Sub 16186 G=0.98332 A=0.01668
gnomAD - Exomes Ashkenazi Jewish Sub 10004 G=0.87445 A=0.12555
gnomAD - Exomes Other Sub 6094 G=0.9042 A=0.0958
Allele Frequency Aggregator Total Global 213118 G=0.889104 A=0.110896
Allele Frequency Aggregator European Sub 181548 G=0.880858 A=0.119142
Allele Frequency Aggregator Other Sub 17134 G=0.90247 A=0.09753
Allele Frequency Aggregator Latin American 2 Sub 5066 G=0.9660 A=0.0340
Allele Frequency Aggregator African Sub 4832 G=0.9774 A=0.0226
Allele Frequency Aggregator Asian Sub 3382 G=0.9982 A=0.0018
Allele Frequency Aggregator Latin American 1 Sub 866 G=0.955 A=0.045
Allele Frequency Aggregator South Asian Sub 290 G=0.976 A=0.024
gnomAD - Genomes Global Study-wide 140160 G=0.908669 A=0.091331
gnomAD - Genomes European Sub 75876 G=0.85702 A=0.14298
gnomAD - Genomes African Sub 42022 G=0.98141 A=0.01859
gnomAD - Genomes American Sub 13660 G=0.95871 A=0.04129
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.8627 A=0.1373
gnomAD - Genomes East Asian Sub 3126 G=0.9994 A=0.0006
gnomAD - Genomes Other Sub 2154 G=0.9308 A=0.0692
ExAC Global Study-wide 117014 G=0.900337 A=0.099663
ExAC Europe Sub 70890 G=0.85070 A=0.14930
ExAC Asian Sub 24414 G=0.98067 A=0.01933
ExAC American Sub 11154 G=0.97050 A=0.02950
ExAC African Sub 9700 G=0.9803 A=0.0197
ExAC Other Sub 856 G=0.900 A=0.100
The PAGE Study Global Study-wide 78512 G=0.97391 A=0.02609
The PAGE Study AfricanAmerican Sub 32376 G=0.97847 A=0.02153
The PAGE Study Mexican Sub 10802 G=0.96621 A=0.03379
The PAGE Study Asian Sub 8310 G=0.9989 A=0.0011
The PAGE Study PuertoRican Sub 7910 G=0.9684 A=0.0316
The PAGE Study NativeHawaiian Sub 4508 G=0.9758 A=0.0242
The PAGE Study Cuban Sub 4230 G=0.9489 A=0.0511
The PAGE Study Dominican Sub 3828 G=0.9639 A=0.0361
The PAGE Study CentralAmerican Sub 2450 G=0.9665 A=0.0335
The PAGE Study SouthAmerican Sub 1982 G=0.9647 A=0.0353
The PAGE Study NativeAmerican Sub 1260 G=0.9302 A=0.0698
The PAGE Study SouthAsian Sub 856 G=0.972 A=0.028
GO Exome Sequencing Project Global Study-wide 12988 G=0.91415 A=0.08585
GO Exome Sequencing Project European American Sub 8588 G=0.8815 A=0.1185
GO Exome Sequencing Project African American Sub 4400 G=0.9780 A=0.0220
1000Genomes_30x Global Study-wide 6404 G=0.9622 A=0.0378
1000Genomes_30x African Sub 1786 G=0.9966 A=0.0034
1000Genomes_30x Europe Sub 1266 G=0.8665 A=0.1335
1000Genomes_30x South Asian Sub 1202 G=0.9817 A=0.0183
1000Genomes_30x East Asian Sub 1170 G=0.9966 A=0.0034
1000Genomes_30x American Sub 980 G=0.958 A=0.042
1000Genomes Global Study-wide 5008 G=0.9603 A=0.0397
1000Genomes African Sub 1322 G=0.9955 A=0.0045
1000Genomes East Asian Sub 1008 G=0.9950 A=0.0050
1000Genomes Europe Sub 1006 G=0.8598 A=0.1402
1000Genomes South Asian Sub 978 G=0.982 A=0.018
1000Genomes American Sub 694 G=0.958 A=0.042
Genetic variation in the Estonian population Estonian Study-wide 4478 G=0.7606 A=0.2394
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.9032 A=0.0968
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.8967 A=0.1033
KOREAN population from KRGDB KOREAN Study-wide 2920 G=0.9997 A=0.0003
A Vietnamese Genetic Variation Database Global Study-wide 614 G=0.997 A=0.003
Northern Sweden ACPOP Study-wide 600 G=0.827 A=0.173
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.979 A=0.021
FINRISK Finnish from FINRISK project Study-wide 270 G=0.741 A=0.259
Qatari Global Study-wide 216 G=0.977 A=0.023
SGDP_PRJ Global Study-wide 58 G=0.45 A=0.55
The Danish reference pan genome Danish Study-wide 40 G=0.85 A=0.15
Siberian Global Study-wide 10 G=0.5 A=0.5
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 11 NC_000011.10:g.69063896G>A
GRCh37.p13 chr 11 NC_000011.9:g.68831364G>A
TPCN2 RefSeqGene NG_016153.2:g.19966G>A
TPCN2 RefSeqGene NG_016153.1:g.20015G>A
Gene: TPCN2, two pore segment channel 2 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
TPCN2 transcript NM_139075.4:c.655G>A V [GTC] > I [ATC] Coding Sequence Variant
two pore channel protein 2 NP_620714.2:p.Val219Ile V (Val) > I (Ile) 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.

Allele: A (allele ID: 1242427 )
ClinVar Accession Disease Names Clinical Significance
RCV001660777.2 not provided Benign
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 G= A
GRCh38.p14 chr 11 NC_000011.10:g.69063896= NC_000011.10:g.69063896G>A
GRCh37.p13 chr 11 NC_000011.9:g.68831364= NC_000011.9:g.68831364G>A
TPCN2 RefSeqGene NG_016153.2:g.19966= NG_016153.2:g.19966G>A
TPCN2 RefSeqGene NG_016153.1:g.20015= NG_016153.1:g.20015G>A
TPCN2 transcript NM_139075.4:c.655= NM_139075.4:c.655G>A
TPCN2 transcript NM_139075.3:c.655= NM_139075.3:c.655G>A
two pore channel protein 2 NP_620714.2:p.Val219= NP_620714.2:p.Val219Ile
TPCN2 transcript variant X7 XM_005273830.1:c.33+906= XM_005273830.1:c.33+906G>A
TPCN2 transcript variant X8 XM_005273831.1:c.33+906= XM_005273831.1:c.33+906G>A
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#.

92 SubSNP, 21 Frequency, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 1000GENOMES ss110611731 Feb 13, 2009 (130)
2 SEATTLESEQ ss159724208 Dec 01, 2009 (131)
3 ILLUMINA ss161042669 Dec 01, 2009 (131)
4 1000GENOMES ss235598741 Jul 15, 2010 (132)
5 GMI ss286401680 Apr 25, 2013 (138)
6 NHLBI-ESP ss342334618 May 09, 2011 (134)
7 ILLUMINA ss479209223 Sep 08, 2015 (146)
8 ILLUMINA ss480739990 May 04, 2012 (137)
9 ILLUMINA ss482876107 May 04, 2012 (137)
10 1000GENOMES ss491024132 May 04, 2012 (137)
11 EXOME_CHIP ss491455279 May 04, 2012 (137)
12 CLINSEQ_SNP ss491649655 May 04, 2012 (137)
13 ILLUMINA ss533916060 Sep 08, 2015 (146)
14 TISHKOFF ss562627179 Apr 25, 2013 (138)
15 SSMP ss658141332 Apr 25, 2013 (138)
16 ILLUMINA ss780901054 Sep 08, 2015 (146)
17 ILLUMINA ss781306243 Sep 08, 2015 (146)
18 ILLUMINA ss783588162 Sep 08, 2015 (146)
19 JMKIDD_LAB ss974480155 Aug 21, 2014 (142)
20 EVA-GONL ss988636472 Aug 21, 2014 (142)
21 JMKIDD_LAB ss1067525863 Aug 21, 2014 (142)
22 1000GENOMES ss1341733497 Aug 21, 2014 (142)
23 EVA_GENOME_DK ss1575774414 Apr 01, 2015 (144)
24 EVA_FINRISK ss1584076571 Apr 01, 2015 (144)
25 EVA_DECODE ss1598298568 Apr 01, 2015 (144)
26 EVA_UK10K_ALSPAC ss1626820267 Apr 01, 2015 (144)
27 EVA_UK10K_TWINSUK ss1669814300 Apr 01, 2015 (144)
28 EVA_EXAC ss1690518281 Apr 01, 2015 (144)
29 EVA_MGP ss1711299995 Apr 01, 2015 (144)
30 ILLUMINA ss1752029514 Sep 08, 2015 (146)
31 ILLUMINA ss1917863168 Feb 12, 2016 (147)
32 WEILL_CORNELL_DGM ss1931995339 Feb 12, 2016 (147)
33 ILLUMINA ss1946314999 Feb 12, 2016 (147)
34 ILLUMINA ss1959361523 Feb 12, 2016 (147)
35 JJLAB ss2026742204 Sep 14, 2016 (149)
36 USC_VALOUEV ss2155049682 Dec 20, 2016 (150)
37 HUMAN_LONGEVITY ss2183255865 Dec 20, 2016 (150)
38 ILLUMINA ss2632846435 Nov 08, 2017 (151)
39 GNOMAD ss2739203803 Nov 08, 2017 (151)
40 GNOMAD ss2748682868 Nov 08, 2017 (151)
41 GNOMAD ss2900986081 Nov 08, 2017 (151)
42 AFFY ss2984948116 Nov 08, 2017 (151)
43 SWEGEN ss3008284531 Nov 08, 2017 (151)
44 ILLUMINA ss3021349112 Nov 08, 2017 (151)
45 BIOINF_KMB_FNS_UNIBA ss3027168569 Nov 08, 2017 (151)
46 CSHL ss3349650159 Nov 08, 2017 (151)
47 ILLUMINA ss3626682280 Oct 12, 2018 (152)
48 ILLUMINA ss3626682281 Oct 12, 2018 (152)
49 ILLUMINA ss3634461356 Oct 12, 2018 (152)
50 ILLUMINA ss3636144497 Oct 12, 2018 (152)
51 ILLUMINA ss3640168695 Oct 12, 2018 (152)
52 ILLUMINA ss3641739348 Oct 12, 2018 (152)
53 ILLUMINA ss3644567804 Oct 12, 2018 (152)
54 OMUKHERJEE_ADBS ss3646429242 Oct 12, 2018 (152)
55 ILLUMINA ss3651714094 Oct 12, 2018 (152)
56 ILLUMINA ss3653720596 Oct 12, 2018 (152)
57 EGCUT_WGS ss3675612328 Jul 13, 2019 (153)
58 EVA_DECODE ss3692007953 Jul 13, 2019 (153)
59 ACPOP ss3738273354 Jul 13, 2019 (153)
60 ILLUMINA ss3744383919 Jul 13, 2019 (153)
61 ILLUMINA ss3744762191 Jul 13, 2019 (153)
62 EVA ss3749434340 Jul 13, 2019 (153)
63 PAGE_CC ss3771633316 Jul 13, 2019 (153)
64 ILLUMINA ss3772262072 Jul 13, 2019 (153)
65 KHV_HUMAN_GENOMES ss3814774394 Jul 13, 2019 (153)
66 EVA ss3824647829 Apr 26, 2020 (154)
67 EVA ss3825803961 Apr 26, 2020 (154)
68 EVA ss3832682927 Apr 26, 2020 (154)
69 EVA ss3839899526 Apr 26, 2020 (154)
70 EVA ss3845379179 Apr 26, 2020 (154)
71 SGDP_PRJ ss3876493912 Apr 26, 2020 (154)
72 KRGDB ss3924887391 Apr 26, 2020 (154)
73 FSA-LAB ss3984007767 Apr 26, 2021 (155)
74 EVA ss3986535425 Apr 26, 2021 (155)
75 TOPMED ss4889271051 Apr 26, 2021 (155)
76 EVA ss5236897216 Apr 26, 2021 (155)
77 EVA ss5237657913 Oct 16, 2022 (156)
78 1000G_HIGH_COVERAGE ss5287825174 Oct 16, 2022 (156)
79 TRAN_CS_UWATERLOO ss5314432532 Oct 16, 2022 (156)
80 EVA ss5315552856 Oct 16, 2022 (156)
81 EVA ss5400301175 Oct 16, 2022 (156)
82 HUGCELL_USP ss5482950141 Oct 16, 2022 (156)
83 1000G_HIGH_COVERAGE ss5583749883 Oct 16, 2022 (156)
84 EVA ss5623954287 Oct 16, 2022 (156)
85 EVA ss5624022989 Oct 16, 2022 (156)
86 SANFORD_IMAGENETICS ss5651449208 Oct 16, 2022 (156)
87 EVA ss5836815475 Oct 16, 2022 (156)
88 EVA ss5847638130 Oct 16, 2022 (156)
89 EVA ss5848330766 Oct 16, 2022 (156)
90 EVA ss5920428612 Oct 16, 2022 (156)
91 EVA ss5936549686 Oct 16, 2022 (156)
92 EVA ss5942760105 Oct 16, 2022 (156)
93 1000Genomes NC_000011.9 - 68831364 Oct 12, 2018 (152)
94 1000Genomes_30x NC_000011.10 - 69063896 Oct 16, 2022 (156)
95 The Avon Longitudinal Study of Parents and Children NC_000011.9 - 68831364 Oct 12, 2018 (152)
96 Genetic variation in the Estonian population NC_000011.9 - 68831364 Oct 12, 2018 (152)
97 ExAC NC_000011.9 - 68831364 Oct 12, 2018 (152)
98 FINRISK NC_000011.9 - 68831364 Apr 26, 2020 (154)
99 The Danish reference pan genome NC_000011.9 - 68831364 Apr 26, 2020 (154)
100 gnomAD - Genomes NC_000011.10 - 69063896 Apr 26, 2021 (155)
101 gnomAD - Exomes NC_000011.9 - 68831364 Jul 13, 2019 (153)
102 GO Exome Sequencing Project NC_000011.9 - 68831364 Oct 12, 2018 (152)
103 KOREAN population from KRGDB NC_000011.9 - 68831364 Apr 26, 2020 (154)
104 Medical Genome Project healthy controls from Spanish population NC_000011.9 - 68831364 Apr 26, 2020 (154)
105 Northern Sweden NC_000011.9 - 68831364 Jul 13, 2019 (153)
106 The PAGE Study NC_000011.10 - 69063896 Jul 13, 2019 (153)
107 Qatari NC_000011.9 - 68831364 Apr 26, 2020 (154)
108 SGDP_PRJ NC_000011.9 - 68831364 Apr 26, 2020 (154)
109 Siberian NC_000011.9 - 68831364 Apr 26, 2020 (154)
110 TopMed NC_000011.10 - 69063896 Apr 26, 2021 (155)
111 UK 10K study - Twins NC_000011.9 - 68831364 Oct 12, 2018 (152)
112 A Vietnamese Genetic Variation Database NC_000011.9 - 68831364 Jul 13, 2019 (153)
113 ALFA NC_000011.10 - 69063896 Apr 26, 2021 (155)
114 ClinVar RCV001660777.2 Oct 16, 2022 (156)
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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss110611731, ss286401680, ss482876107, ss491649655, ss1598298568 NC_000011.8:68587939:G:A NC_000011.10:69063895:G:A (self)
54271691, 30127863, 21350576, 784889, 73032, 2609842, 8419854, 1105399, 32064785, 415755, 11558219, 14037269, 28510892, 7566036, 30127863, 6685020, ss235598741, ss342334618, ss479209223, ss480739990, ss491024132, ss491455279, ss533916060, ss562627179, ss658141332, ss780901054, ss781306243, ss783588162, ss974480155, ss988636472, ss1067525863, ss1341733497, ss1575774414, ss1584076571, ss1626820267, ss1669814300, ss1690518281, ss1711299995, ss1752029514, ss1917863168, ss1931995339, ss1946314999, ss1959361523, ss2026742204, ss2155049682, ss2632846435, ss2739203803, ss2748682868, ss2900986081, ss2984948116, ss3008284531, ss3021349112, ss3349650159, ss3626682280, ss3626682281, ss3634461356, ss3636144497, ss3640168695, ss3641739348, ss3644567804, ss3646429242, ss3651714094, ss3653720596, ss3675612328, ss3738273354, ss3744383919, ss3744762191, ss3749434340, ss3772262072, ss3824647829, ss3825803961, ss3832682927, ss3839899526, ss3876493912, ss3924887391, ss3984007767, ss3986535425, ss5315552856, ss5400301175, ss5623954287, ss5624022989, ss5651449208, ss5836815475, ss5847638130, ss5848330766, ss5936549686, ss5942760105 NC_000011.9:68831363:G:A NC_000011.10:69063895:G:A (self)
RCV001660777.2, 71275818, 383106279, 854785, 104816707, 7804681451, ss2183255865, ss3027168569, ss3692007953, ss3771633316, ss3814774394, ss3845379179, ss4889271051, ss5236897216, ss5237657913, ss5287825174, ss5314432532, ss5482950141, ss5583749883, ss5920428612 NC_000011.10:69063895:G:A NC_000011.10:69063895:G:A (self)
ss159724208, ss161042669 NT_167190.1:14137158:G:A NC_000011.10:69063895:G:A (self)
Help

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

1 citation for rs72928978
PMID Title Author Year Journal
33692100 Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color. Simcoe M et al. 2021 Science advances
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