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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.

rs41301825

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr20:34292436 (GRCh38.p13) 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
C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.004371 (1157/264690, TOPMED)
T=0.003822 (961/251466, GnomAD_exome)
T=0.006376 (1424/223338, ALFA) (+ 16 more)
T=0.004056 (569/140278, GnomAD)
T=0.004056 (492/121292, ExAC)
T=0.00217 (169/77808, PAGE_STUDY)
T=0.00006 (1/16760, 8.3KJPN)
T=0.00461 (60/13006, GO-ESP)
T=0.0032 (16/5008, 1000G)
T=0.0027 (12/4480, Estonian)
T=0.0062 (24/3854, ALSPAC)
T=0.0051 (19/3708, TWINSUK)
T=0.010 (10/998, GoNL)
T=0.002 (1/600, NorthernSweden)
T=0.009 (5/534, MGP)
T=0.006 (3/526, PharmGKB)
T=0.003 (1/304, FINRISK)
C=0.5 (1/2, SGDP_PRJ)
T=0.5 (1/2, SGDP_PRJ)
Clinical Significance
Reported in ClinVar
Gene : Consequence
AHCY : Missense 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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 223338 C=0.993624 T=0.006376
European Sub 193764 C=0.993172 T=0.006828
African Sub 4946 C=0.9990 T=0.0010
African Others Sub 176 C=1.000 T=0.000
African American Sub 4770 C=0.9990 T=0.0010
Asian Sub 6336 C=1.0000 T=0.0000
East Asian Sub 4492 C=1.0000 T=0.0000
Other Asian Sub 1844 C=1.0000 T=0.0000
Latin American 1 Sub 794 C=0.994 T=0.006
Latin American 2 Sub 964 C=0.997 T=0.003
South Asian Sub 280 C=1.000 T=0.000
Other Sub 16254 C=0.99459 T=0.00541


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 C=0.995629 T=0.004371
gnomAD - Exomes Global Study-wide 251466 C=0.996178 T=0.003822
gnomAD - Exomes European Sub 135396 C=0.994557 T=0.005443
gnomAD - Exomes Asian Sub 49006 C=0.99939 T=0.00061
gnomAD - Exomes American Sub 34592 C=0.99720 T=0.00280
gnomAD - Exomes African Sub 16256 C=0.99895 T=0.00105
gnomAD - Exomes Ashkenazi Jewish Sub 10080 C=0.99504 T=0.00496
gnomAD - Exomes Other Sub 6136 C=0.9951 T=0.0049
Allele Frequency Aggregator Total Global 223338 C=0.993624 T=0.006376
Allele Frequency Aggregator European Sub 193764 C=0.993172 T=0.006828
Allele Frequency Aggregator Other Sub 16254 C=0.99459 T=0.00541
Allele Frequency Aggregator Asian Sub 6336 C=1.0000 T=0.0000
Allele Frequency Aggregator African Sub 4946 C=0.9990 T=0.0010
Allele Frequency Aggregator Latin American 2 Sub 964 C=0.997 T=0.003
Allele Frequency Aggregator Latin American 1 Sub 794 C=0.994 T=0.006
Allele Frequency Aggregator South Asian Sub 280 C=1.000 T=0.000
gnomAD - Genomes Global Study-wide 140278 C=0.995944 T=0.004056
gnomAD - Genomes European Sub 75944 C=0.99380 T=0.00620
gnomAD - Genomes African Sub 42058 C=0.99900 T=0.00100
gnomAD - Genomes American Sub 13666 C=0.99795 T=0.00205
gnomAD - Genomes Ashkenazi Jewish Sub 3324 C=0.9946 T=0.0054
gnomAD - Genomes East Asian Sub 3132 C=1.0000 T=0.0000
gnomAD - Genomes Other Sub 2154 C=0.9954 T=0.0046
ExAC Global Study-wide 121292 C=0.995944 T=0.004056
ExAC Europe Sub 73294 C=0.99426 T=0.00574
ExAC Asian Sub 25152 C=0.99920 T=0.00080
ExAC American Sub 11558 C=0.99663 T=0.00337
ExAC African Sub 10384 C=0.99904 T=0.00096
ExAC Other Sub 904 C=0.998 T=0.002
The PAGE Study Global Study-wide 77808 C=0.99783 T=0.00217
The PAGE Study AfricanAmerican Sub 32070 C=0.99897 T=0.00103
The PAGE Study Mexican Sub 10740 C=0.99702 T=0.00298
The PAGE Study Asian Sub 8202 C=0.9996 T=0.0004
The PAGE Study PuertoRican Sub 7852 C=0.9964 T=0.0036
The PAGE Study NativeHawaiian Sub 4458 C=0.9975 T=0.0025
The PAGE Study Cuban Sub 4214 C=0.9941 T=0.0059
The PAGE Study Dominican Sub 3776 C=0.9971 T=0.0029
The PAGE Study CentralAmerican Sub 2436 C=0.9988 T=0.0012
The PAGE Study SouthAmerican Sub 1978 C=0.9934 T=0.0066
The PAGE Study NativeAmerican Sub 1256 C=0.9936 T=0.0064
The PAGE Study SouthAsian Sub 826 C=0.998 T=0.002
8.3KJPN JAPANESE Study-wide 16760 C=0.99994 T=0.00006
GO Exome Sequencing Project Global Study-wide 13006 C=0.99539 T=0.00461
GO Exome Sequencing Project European American Sub 8600 C=0.9935 T=0.0065
GO Exome Sequencing Project African American Sub 4406 C=0.9991 T=0.0009
1000Genomes Global Study-wide 5008 C=0.9968 T=0.0032
1000Genomes African Sub 1322 C=1.0000 T=0.0000
1000Genomes East Asian Sub 1008 C=1.0000 T=0.0000
1000Genomes Europe Sub 1006 C=0.9901 T=0.0099
1000Genomes South Asian Sub 978 C=0.999 T=0.001
1000Genomes American Sub 694 C=0.993 T=0.007
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.9973 T=0.0027
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.9938 T=0.0062
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.9949 T=0.0051
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.990 T=0.010
Northern Sweden ACPOP Study-wide 600 C=0.998 T=0.002
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 C=0.991 T=0.009
PharmGKB Aggregated Global Study-wide 526 C=0.994 T=0.006
PharmGKB Aggregated PA151057141 Sub 526 C=0.994 T=0.006
FINRISK Finnish from FINRISK project Study-wide 304 C=0.997 T=0.003
SGDP_PRJ Global Study-wide 2 C=0.5 T=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.p13 chr 20 NC_000020.11:g.34292436C>T
GRCh37.p13 chr 20 NC_000020.10:g.32880242C>T
AHCY RefSeqGene NG_012630.2:g.24367G>A
Gene: AHCY, adenosylhomocysteinase (minus strand)
Molecule type Change Amino acid[Codon] SO Term
AHCY transcript variant 1 NM_000687.4:c.367G>A G [GGG] > R [AGG] Coding Sequence Variant
adenosylhomocysteinase isoform 1 NP_000678.1:p.Gly123Arg G (Gly) > R (Arg) Missense Variant
AHCY transcript variant 5 NM_001322085.2:c.283G>A G [GGG] > R [AGG] Coding Sequence Variant
adenosylhomocysteinase isoform 2 NP_001309014.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
AHCY transcript variant 3 NM_001322086.2:c.373G>A G [GGG] > R [AGG] Coding Sequence Variant
adenosylhomocysteinase isoform 3 NP_001309015.1:p.Gly125Arg G (Gly) > R (Arg) Missense Variant
AHCY transcript variant 6 NM_001362750.2:c.367G>A G [GGG] > R [AGG] Coding Sequence Variant
adenosylhomocysteinase isoform 1 NP_001349679.1:p.Gly123Arg G (Gly) > R (Arg) Missense Variant
AHCY transcript variant 4 NM_001322084.2:c.283G>A G [GGG] > R [AGG] Coding Sequence Variant
adenosylhomocysteinase isoform 2 NP_001309013.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
AHCY transcript variant 2 NM_001161766.2:c.283G>A G [GGG] > R [AGG] Coding Sequence Variant
adenosylhomocysteinase isoform 2 NP_001155238.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
AHCY transcript variant X8 XM_017027710.2:c.-12= N/A 5 Prime UTR Variant
AHCY transcript variant X7 XM_011528659.1:c.283G>A G [GGG] > R [AGG] Coding Sequence Variant
adenosylhomocysteinase isoform X2 XP_011526961.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
AHCY transcript variant X2 XM_011528657.2:c.373G>A G [GGG] > R [AGG] Coding Sequence Variant
adenosylhomocysteinase isoform X1 XP_011526959.2:p.Gly125Arg G (Gly) > R (Arg) Missense Variant
AHCY transcript variant X6 XM_005260317.2:c.283G>A G [GGG] > R [AGG] Coding Sequence Variant
adenosylhomocysteinase isoform X3 XP_005260374.1:p.Gly95Arg G (Gly) > R (Arg) Missense Variant
AHCY transcript variant X1 XM_011528656.3:c.373G>A G [GGG] > R [AGG] Coding Sequence Variant
adenosylhomocysteinase isoform X1 XP_011526958.2:p.Gly125Arg G (Gly) > R (Arg) Missense Variant
AHCY transcript variant X3 XM_011528658.3:c.373G>A G [GGG] > R [AGG] Coding Sequence Variant
adenosylhomocysteinase isoform X1 XP_011526960.2:p.Gly125Arg G (Gly) > R (Arg) Missense Variant
AHCY transcript variant X5 XM_017027709.2:c.367G>A G [GGG] > R [AGG] Coding Sequence Variant
adenosylhomocysteinase isoform X1 XP_016883198.1:p.Gly123Arg G (Gly) > 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.

Allele: T (allele ID: 533553 )
ClinVar Accession Disease Names Clinical Significance
RCV000648703.4 Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency Likely-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 C= T
GRCh38.p13 chr 20 NC_000020.11:g.34292436= NC_000020.11:g.34292436C>T
GRCh37.p13 chr 20 NC_000020.10:g.32880242= NC_000020.10:g.32880242C>T
AHCY RefSeqGene NG_012630.2:g.24367= NG_012630.2:g.24367G>A
AHCY transcript variant 1 NM_000687.4:c.367= NM_000687.4:c.367G>A
AHCY transcript variant 1 NM_000687.3:c.367= NM_000687.3:c.367G>A
AHCY transcript variant 1 NM_000687.2:c.367= NM_000687.2:c.367G>A
AHCY transcript variant 3 NM_001322086.2:c.373= NM_001322086.2:c.373G>A
AHCY transcript variant 3 NM_001322086.1:c.373= NM_001322086.1:c.373G>A
AHCY transcript variant 4 NM_001322084.2:c.283= NM_001322084.2:c.283G>A
AHCY transcript variant 4 NM_001322084.1:c.283= NM_001322084.1:c.283G>A
AHCY transcript variant 5 NM_001322085.2:c.283= NM_001322085.2:c.283G>A
AHCY transcript variant 5 NM_001322085.1:c.283= NM_001322085.1:c.283G>A
AHCY transcript variant 6 NM_001362750.2:c.367= NM_001362750.2:c.367G>A
AHCY transcript variant 6 NM_001362750.1:c.367= NM_001362750.1:c.367G>A
AHCY transcript variant 2 NM_001161766.1:c.283= NM_001161766.1:c.283G>A
AHCY transcript variant 2 NM_001161766.2:c.283= NM_001161766.2:c.283G>A
AHCY transcript variant X1 XM_011528656.3:c.373= XM_011528656.3:c.373G>A
AHCY transcript variant X3 XM_011528658.3:c.373= XM_011528658.3:c.373G>A
AHCY transcript variant X6 XM_005260317.2:c.283= XM_005260317.2:c.283G>A
AHCY transcript variant X5 XM_005260317.1:c.283= XM_005260317.1:c.283G>A
AHCY transcript variant X8 XM_017027710.2:c.-12= XM_017027710.2:c.-12G>A
AHCY transcript variant X5 XM_017027709.2:c.367= XM_017027709.2:c.367G>A
AHCY transcript variant X2 XM_011528657.2:c.373= XM_011528657.2:c.373G>A
AHCY transcript variant X7 XM_011528659.1:c.283= XM_011528659.1:c.283G>A
adenosylhomocysteinase isoform 1 NP_000678.1:p.Gly123= NP_000678.1:p.Gly123Arg
adenosylhomocysteinase isoform 3 NP_001309015.1:p.Gly125= NP_001309015.1:p.Gly125Arg
adenosylhomocysteinase isoform 2 NP_001309013.1:p.Gly95= NP_001309013.1:p.Gly95Arg
adenosylhomocysteinase isoform 2 NP_001309014.1:p.Gly95= NP_001309014.1:p.Gly95Arg
adenosylhomocysteinase isoform 1 NP_001349679.1:p.Gly123= NP_001349679.1:p.Gly123Arg
adenosylhomocysteinase isoform 2 NP_001155238.1:p.Gly95= NP_001155238.1:p.Gly95Arg
adenosylhomocysteinase isoform X1 XP_011526958.2:p.Gly125= XP_011526958.2:p.Gly125Arg
adenosylhomocysteinase isoform X1 XP_011526960.2:p.Gly125= XP_011526960.2:p.Gly125Arg
adenosylhomocysteinase isoform X3 XP_005260374.1:p.Gly95= XP_005260374.1:p.Gly95Arg
adenosylhomocysteinase isoform X1 XP_016883198.1:p.Gly123= XP_016883198.1:p.Gly123Arg
adenosylhomocysteinase isoform X1 XP_011526959.2:p.Gly125= XP_011526959.2:p.Gly125Arg
adenosylhomocysteinase isoform X2 XP_011526961.1:p.Gly95= XP_011526961.1:p.Gly95Arg
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#.

57 SubSNP, 18 Frequency, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 SI_EXO ss61707691 Oct 18, 2006 (127)
2 PHARMGKB_PPII ss84170262 Dec 15, 2007 (130)
3 CORNELL ss86245977 Mar 23, 2008 (130)
4 1000GENOMES ss237819117 Jul 15, 2010 (132)
5 NHLBI-ESP ss342519872 May 09, 2011 (134)
6 ILLUMINA ss480698215 May 04, 2012 (137)
7 ILLUMINA ss484181008 May 04, 2012 (137)
8 1000GENOMES ss491175445 May 04, 2012 (137)
9 EXOME_CHIP ss491559816 May 04, 2012 (137)
10 CLINSEQ_SNP ss491808289 May 04, 2012 (137)
11 ILLUMINA ss780753936 Sep 08, 2015 (146)
12 ILLUMINA ss781295757 Sep 11, 2015 (146)
13 ILLUMINA ss783432198 Sep 08, 2015 (146)
14 EVA-GONL ss994684151 Aug 21, 2014 (142)
15 1000GENOMES ss1364626828 Aug 21, 2014 (142)
16 EVA_FINRISK ss1584122559 Apr 01, 2015 (144)
17 EVA_UK10K_ALSPAC ss1638703079 Apr 01, 2015 (144)
18 EVA_UK10K_TWINSUK ss1681697112 Apr 01, 2015 (144)
19 EVA_EXAC ss1693959400 Apr 01, 2015 (144)
20 EVA_DECODE ss1698742844 Apr 01, 2015 (144)
21 EVA_MGP ss1711538848 Apr 01, 2015 (144)
22 ILLUMINA ss1752383595 Sep 08, 2015 (146)
23 ILLUMINA ss1917946282 Feb 12, 2016 (147)
24 ILLUMINA ss1946550727 Feb 12, 2016 (147)
25 ILLUMINA ss1959911476 Feb 12, 2016 (147)
26 JJLAB ss2029881132 Sep 14, 2016 (149)
27 HUMAN_LONGEVITY ss2242448390 Dec 20, 2016 (150)
28 TOPMED ss2408976471 Dec 20, 2016 (150)
29 ILLUMINA ss2710938522 Nov 08, 2017 (151)
30 GNOMAD ss2744549230 Nov 08, 2017 (151)
31 GNOMAD ss2750365453 Nov 08, 2017 (151)
32 GNOMAD ss2967005597 Nov 08, 2017 (151)
33 AFFY ss2985213601 Nov 08, 2017 (151)
34 SWEGEN ss3018127361 Nov 08, 2017 (151)
35 ILLUMINA ss3022115094 Nov 08, 2017 (151)
36 TOPMED ss3359490504 Nov 08, 2017 (151)
37 ILLUMINA ss3628382430 Oct 12, 2018 (152)
38 ILLUMINA ss3634833559 Oct 12, 2018 (152)
39 ILLUMINA ss3640540857 Oct 12, 2018 (152)
40 ILLUMINA ss3644781113 Oct 12, 2018 (152)
41 ILLUMINA ss3652570106 Oct 12, 2018 (152)
42 ILLUMINA ss3653982369 Oct 12, 2018 (152)
43 EGCUT_WGS ss3684806837 Jul 13, 2019 (153)
44 EVA_DECODE ss3706875114 Jul 13, 2019 (153)
45 ILLUMINA ss3725911678 Jul 13, 2019 (153)
46 ACPOP ss3743365010 Jul 13, 2019 (153)
47 ILLUMINA ss3744492779 Jul 13, 2019 (153)
48 ILLUMINA ss3745133456 Jul 13, 2019 (153)
49 PAGE_CC ss3772045099 Jul 13, 2019 (153)
50 ILLUMINA ss3772629675 Jul 13, 2019 (153)
51 EVA ss3825363423 Apr 27, 2020 (154)
52 EVA ss3825951264 Apr 27, 2020 (154)
53 SGDP_PRJ ss3889029333 Apr 27, 2020 (154)
54 NORTHRUP_AU ss3983909676 Apr 26, 2021 (155)
55 EVA ss3986828463 Apr 26, 2021 (155)
56 TOPMED ss5087331586 Apr 26, 2021 (155)
57 TOMMO_GENOMICS ss5229478194 Apr 26, 2021 (155)
58 1000Genomes NC_000020.10 - 32880242 Oct 12, 2018 (152)
59 The Avon Longitudinal Study of Parents and Children NC_000020.10 - 32880242 Oct 12, 2018 (152)
60 Genetic variation in the Estonian population NC_000020.10 - 32880242 Oct 12, 2018 (152)
61 ExAC NC_000020.10 - 32880242 Oct 12, 2018 (152)
62 FINRISK NC_000020.10 - 32880242 Apr 27, 2020 (154)
63 gnomAD - Genomes NC_000020.11 - 34292436 Apr 26, 2021 (155)
64 gnomAD - Exomes NC_000020.10 - 32880242 Jul 13, 2019 (153)
65 GO Exome Sequencing Project NC_000020.10 - 32880242 Oct 12, 2018 (152)
66 Genome of the Netherlands Release 5 NC_000020.10 - 32880242 Apr 27, 2020 (154)
67 Medical Genome Project healthy controls from Spanish population NC_000020.10 - 32880242 Apr 27, 2020 (154)
68 Northern Sweden NC_000020.10 - 32880242 Jul 13, 2019 (153)
69 The PAGE Study NC_000020.11 - 34292436 Jul 13, 2019 (153)
70 PharmGKB Aggregated NC_000020.11 - 34292436 Apr 27, 2020 (154)
71 SGDP_PRJ NC_000020.10 - 32880242 Apr 27, 2020 (154)
72 8.3KJPN NC_000020.10 - 32880242 Apr 26, 2021 (155)
73 TopMed NC_000020.11 - 34292436 Apr 26, 2021 (155)
74 UK 10K study - Twins NC_000020.10 - 32880242 Oct 12, 2018 (152)
75 ALFA NC_000020.11 - 34292436 Apr 26, 2021 (155)
76 ClinVar RCV000648703.4 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)
rs60407722 May 26, 2008 (130)
rs61730991 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss484181008, ss491808289, ss1698742844 NC_000020.9:32343902:C:T NC_000020.11:34292435:C:T (self)
78085112, 43223133, 30545085, 5511531, 119020, 13869482, 1820326, 19258506, 654608, 16649875, 41046313, 87447501, 43223133, ss237819117, ss342519872, ss480698215, ss491175445, ss491559816, ss780753936, ss781295757, ss783432198, ss994684151, ss1364626828, ss1584122559, ss1638703079, ss1681697112, ss1693959400, ss1711538848, ss1752383595, ss1917946282, ss1946550727, ss1959911476, ss2029881132, ss2408976471, ss2710938522, ss2744549230, ss2750365453, ss2967005597, ss2985213601, ss3018127361, ss3022115094, ss3628382430, ss3634833559, ss3640540857, ss3644781113, ss3652570106, ss3653982369, ss3684806837, ss3743365010, ss3744492779, ss3745133456, ss3772629675, ss3825363423, ss3825951264, ss3889029333, ss3983909676, ss3986828463, ss5229478194 NC_000020.10:32880241:C:T NC_000020.11:34292435:C:T (self)
RCV000648703.4, 550792985, 1266568, 7129, 226324997, 362440531, 13054696000, ss2242448390, ss3359490504, ss3706875114, ss3725911678, ss3772045099, ss5087331586 NC_000020.11:34292435:C:T NC_000020.11:34292435:C:T (self)
ss84170262, ss86245977 NT_011362.10:3076333:C:T NC_000020.11:34292435:C:T (self)
ss61707691 NT_028392.5:3076333:C:T NC_000020.11:34292435:C:T (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 rs41301825

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.post676+237644a