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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.

rs1859927

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr2:241082956 (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
T>A / T>C / T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.364328 (96434/264690, TOPMED)
C=0.336838 (47028/139616, GnomAD)
T=0.44822 (12665/28256, 14KJPN) (+ 15 more)
C=0.23370 (4982/21318, ALFA)
T=0.44110 (7392/16758, 8.3KJPN)
C=0.4257 (2132/5008, 1000G)
C=0.1487 (573/3854, ALSPAC)
C=0.1575 (584/3708, TWINSUK)
T=0.4648 (1362/2930, KOREAN)
T=0.4733 (867/1832, Korea1K)
C=0.152 (152/998, GoNL)
C=0.153 (92/600, NorthernSweden)
T=0.291 (102/350, SGDP_PRJ)
C=0.338 (73/216, Qatari)
T=0.458 (98/214, Vietnamese)
C=0.15 (6/40, GENOME_DK)
T=0.50 (14/28, Siberian)
C=0.50 (14/28, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
MTERF4 : Intron Variant
SNED1 : 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 21318 T=0.76630 A=0.00000, C=0.23370, G=0.00000
European Sub 16892 T=0.84099 A=0.00000, C=0.15901, G=0.00000
African Sub 2552 T=0.3456 A=0.0000, C=0.6544, G=0.0000
African Others Sub 96 T=0.14 A=0.00, C=0.86, G=0.00
African American Sub 2456 T=0.3538 A=0.0000, C=0.6462, G=0.0000
Asian Sub 120 T=0.492 A=0.000, C=0.508, G=0.000
East Asian Sub 94 T=0.50 A=0.00, C=0.50, G=0.00
Other Asian Sub 26 T=0.46 A=0.00, C=0.54, G=0.00
Latin American 1 Sub 148 T=0.595 A=0.000, C=0.405, G=0.000
Latin American 2 Sub 622 T=0.645 A=0.000, C=0.355, G=0.000
South Asian Sub 106 T=0.849 A=0.000, C=0.151, G=0.000
Other Sub 878 T=0.695 A=0.000, C=0.305, G=0.000


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 T=0.635672 C=0.364328
gnomAD - Genomes Global Study-wide 139616 T=0.663162 C=0.336838
gnomAD - Genomes European Sub 75606 T=0.84343 C=0.15657
gnomAD - Genomes African Sub 41882 T=0.33384 C=0.66616
gnomAD - Genomes American Sub 13554 T=0.69706 C=0.30294
gnomAD - Genomes Ashkenazi Jewish Sub 3316 T=0.7723 C=0.2277
gnomAD - Genomes East Asian Sub 3120 T=0.4385 C=0.5615
gnomAD - Genomes Other Sub 2138 T=0.6833 C=0.3167
14KJPN JAPANESE Study-wide 28256 T=0.44822 C=0.55178
Allele Frequency Aggregator Total Global 21318 T=0.76630 A=0.00000, C=0.23370, G=0.00000
Allele Frequency Aggregator European Sub 16892 T=0.84099 A=0.00000, C=0.15901, G=0.00000
Allele Frequency Aggregator African Sub 2552 T=0.3456 A=0.0000, C=0.6544, G=0.0000
Allele Frequency Aggregator Other Sub 878 T=0.695 A=0.000, C=0.305, G=0.000
Allele Frequency Aggregator Latin American 2 Sub 622 T=0.645 A=0.000, C=0.355, G=0.000
Allele Frequency Aggregator Latin American 1 Sub 148 T=0.595 A=0.000, C=0.405, G=0.000
Allele Frequency Aggregator Asian Sub 120 T=0.492 A=0.000, C=0.508, G=0.000
Allele Frequency Aggregator South Asian Sub 106 T=0.849 A=0.000, C=0.151, G=0.000
8.3KJPN JAPANESE Study-wide 16758 T=0.44110 C=0.55890
1000Genomes Global Study-wide 5008 T=0.5743 C=0.4257
1000Genomes African Sub 1322 T=0.2489 C=0.7511
1000Genomes East Asian Sub 1008 T=0.4484 C=0.5516
1000Genomes Europe Sub 1006 T=0.8310 C=0.1690
1000Genomes South Asian Sub 978 T=0.829 C=0.171
1000Genomes American Sub 694 T=0.646 C=0.354
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.8513 C=0.1487
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.8425 C=0.1575
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.4648 C=0.5352
Korean Genome Project KOREAN Study-wide 1832 T=0.4733 C=0.5267
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.848 C=0.152
Northern Sweden ACPOP Study-wide 600 T=0.847 C=0.153
SGDP_PRJ Global Study-wide 350 T=0.291 C=0.709
Qatari Global Study-wide 216 T=0.662 C=0.338
A Vietnamese Genetic Variation Database Global Study-wide 214 T=0.458 C=0.542
The Danish reference pan genome Danish Study-wide 40 T=0.85 C=0.15
Siberian Global Study-wide 28 T=0.50 C=0.50
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 2 NC_000002.12:g.241082956T>A
GRCh38.p14 chr 2 NC_000002.12:g.241082956T>C
GRCh38.p14 chr 2 NC_000002.12:g.241082956T>G
GRCh37.p13 chr 2 NC_000002.11:g.242022371T>A
GRCh37.p13 chr 2 NC_000002.11:g.242022371T>C
GRCh37.p13 chr 2 NC_000002.11:g.242022371T>G
Gene: SNED1, sushi, nidogen and EGF like domains 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
SNED1 transcript NM_001080437.3:c.4121+592…

NM_001080437.3:c.4121+592T>A

N/A Intron Variant
SNED1 transcript variant X2 XM_011510931.3:c.4193+592…

XM_011510931.3:c.4193+592T>A

N/A Intron Variant
SNED1 transcript variant X7 XM_011510932.3:c.4094+592…

XM_011510932.3:c.4094+592T>A

N/A Intron Variant
SNED1 transcript variant X3 XM_047443884.1:c.4193+592…

XM_047443884.1:c.4193+592T>A

N/A Intron Variant
SNED1 transcript variant X8 XM_047443885.1:c.4079+592…

XM_047443885.1:c.4079+592T>A

N/A Intron Variant
SNED1 transcript variant X10 XM_047443886.1:c.4022+592…

XM_047443886.1:c.4022+592T>A

N/A Intron Variant
SNED1 transcript variant X11 XM_047443887.1:c.4007+592…

XM_047443887.1:c.4007+592T>A

N/A Intron Variant
SNED1 transcript variant X12 XM_047443888.1:c.3980+592…

XM_047443888.1:c.3980+592T>A

N/A Intron Variant
SNED1 transcript variant X14 XM_047443889.1:c.3908+592…

XM_047443889.1:c.3908+592T>A

N/A Intron Variant
SNED1 transcript variant X15 XM_011510934.4:c. N/A Genic Downstream Transcript Variant
SNED1 transcript variant X22 XM_011510937.3:c. N/A Genic Downstream Transcript Variant
SNED1 transcript variant X13 XM_024452784.2:c. N/A Genic Downstream Transcript Variant
SNED1 transcript variant X19 XM_047443890.1:c. N/A Genic Downstream Transcript Variant
SNED1 transcript variant X20 XM_047443891.1:c. N/A Genic Downstream Transcript Variant
SNED1 transcript variant X1 XR_002959254.2:n. N/A Intron Variant
SNED1 transcript variant X4 XR_002959255.2:n. N/A Intron Variant
SNED1 transcript variant X5 XR_002959256.2:n. N/A Intron Variant
SNED1 transcript variant X6 XR_002959257.2:n. N/A Intron Variant
SNED1 transcript variant X9 XR_002959258.2:n. N/A Intron Variant
SNED1 transcript variant X18 XR_002959260.2:n. N/A Intron Variant
SNED1 transcript variant X16 XR_002959262.2:n. N/A Intron Variant
SNED1 transcript variant X21 XR_002959263.2:n. N/A Intron Variant
SNED1 transcript variant X17 XR_007071512.1:n. N/A Intron Variant
Gene: MTERF4, mitochondrial transcription termination factor 4 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
MTERF4 transcript variant 5 NM_001330179.2:c. N/A Genic Downstream Transcript Variant
MTERF4 transcript variant 6 NM_001330180.2:c. N/A Genic Downstream Transcript Variant
MTERF4 transcript variant 1 NM_182501.4:c. N/A Genic Downstream Transcript Variant
MTERF4 transcript variant 7 NR_138463.2:n. N/A Intron Variant
MTERF4 transcript variant 2 NR_028049.2:n. N/A Genic Downstream Transcript Variant
MTERF4 transcript variant 3 NR_028050.2:n. N/A Genic Downstream Transcript Variant
MTERF4 transcript variant 4 NR_028051.2:n. N/A Genic Downstream Transcript Variant
MTERF4 transcript variant 8 NR_138464.2:n. N/A Genic Downstream Transcript Variant
MTERF4 transcript variant 9 NR_138465.2:n. N/A Genic Downstream Transcript Variant
MTERF4 transcript variant 10 NR_138466.2:n. N/A Genic Downstream Transcript Variant
MTERF4 transcript variant X1 XM_047443427.1:c.*160+623…

XM_047443427.1:c.*160+6232A>T

N/A Intron Variant
MTERF4 transcript variant X2 XM_047443428.1:c.*160+623…

XM_047443428.1:c.*160+6232A>T

N/A Intron Variant
MTERF4 transcript variant X3 XM_047443429.1:c. N/A Genic Downstream Transcript 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 T= A C G
GRCh38.p14 chr 2 NC_000002.12:g.241082956= NC_000002.12:g.241082956T>A NC_000002.12:g.241082956T>C NC_000002.12:g.241082956T>G
GRCh37.p13 chr 2 NC_000002.11:g.242022371= NC_000002.11:g.242022371T>A NC_000002.11:g.242022371T>C NC_000002.11:g.242022371T>G
SNED1 transcript NM_001080437.1:c.4121+592= NM_001080437.1:c.4121+592T>A NM_001080437.1:c.4121+592T>C NM_001080437.1:c.4121+592T>G
SNED1 transcript NM_001080437.3:c.4121+592= NM_001080437.3:c.4121+592T>A NM_001080437.3:c.4121+592T>C NM_001080437.3:c.4121+592T>G
SNED1 transcript variant X1 XM_005246997.1:c.4121+592= XM_005246997.1:c.4121+592T>A XM_005246997.1:c.4121+592T>C XM_005246997.1:c.4121+592T>G
SNED1 transcript variant X2 XM_005246998.1:c.4121+592= XM_005246998.1:c.4121+592T>A XM_005246998.1:c.4121+592T>C XM_005246998.1:c.4121+592T>G
SNED1 transcript variant X2 XM_011510931.3:c.4193+592= XM_011510931.3:c.4193+592T>A XM_011510931.3:c.4193+592T>C XM_011510931.3:c.4193+592T>G
SNED1 transcript variant X7 XM_011510932.3:c.4094+592= XM_011510932.3:c.4094+592T>A XM_011510932.3:c.4094+592T>C XM_011510932.3:c.4094+592T>G
MTERF4 transcript variant X1 XM_047443427.1:c.*160+6232= XM_047443427.1:c.*160+6232A>T XM_047443427.1:c.*160+6232A>G XM_047443427.1:c.*160+6232A>C
MTERF4 transcript variant X2 XM_047443428.1:c.*160+6232= XM_047443428.1:c.*160+6232A>T XM_047443428.1:c.*160+6232A>G XM_047443428.1:c.*160+6232A>C
SNED1 transcript variant X3 XM_047443884.1:c.4193+592= XM_047443884.1:c.4193+592T>A XM_047443884.1:c.4193+592T>C XM_047443884.1:c.4193+592T>G
SNED1 transcript variant X8 XM_047443885.1:c.4079+592= XM_047443885.1:c.4079+592T>A XM_047443885.1:c.4079+592T>C XM_047443885.1:c.4079+592T>G
SNED1 transcript variant X10 XM_047443886.1:c.4022+592= XM_047443886.1:c.4022+592T>A XM_047443886.1:c.4022+592T>C XM_047443886.1:c.4022+592T>G
SNED1 transcript variant X11 XM_047443887.1:c.4007+592= XM_047443887.1:c.4007+592T>A XM_047443887.1:c.4007+592T>C XM_047443887.1:c.4007+592T>G
SNED1 transcript variant X12 XM_047443888.1:c.3980+592= XM_047443888.1:c.3980+592T>A XM_047443888.1:c.3980+592T>C XM_047443888.1:c.3980+592T>G
SNED1 transcript variant X14 XM_047443889.1:c.3908+592= XM_047443889.1:c.3908+592T>A XM_047443889.1:c.3908+592T>C XM_047443889.1:c.3908+592T>G
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#.

73 SubSNP, 17 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss2733695 Jan 12, 2001 (92)
2 BCM_SSAHASNP ss9953093 Jul 11, 2003 (116)
3 WUGSC_SSAHASNP ss14467604 Dec 05, 2003 (119)
4 ABI ss41563131 Mar 15, 2006 (126)
5 HGSV ss81723329 Dec 14, 2007 (130)
6 HGSV ss82164069 Dec 14, 2007 (130)
7 BCMHGSC_JDW ss91608771 Mar 24, 2008 (129)
8 BGI ss103709655 Dec 01, 2009 (131)
9 ILLUMINA-UK ss118150077 Feb 14, 2009 (130)
10 ENSEMBL ss138660795 Dec 01, 2009 (131)
11 GMI ss154949609 Dec 01, 2009 (131)
12 COMPLETE_GENOMICS ss165809414 Jul 04, 2010 (132)
13 BUSHMAN ss201979484 Jul 04, 2010 (132)
14 1000GENOMES ss210524318 Jul 14, 2010 (132)
15 1000GENOMES ss219918270 Jul 14, 2010 (132)
16 1000GENOMES ss231661746 Jul 14, 2010 (132)
17 1000GENOMES ss239104967 Jul 15, 2010 (132)
18 GMI ss276967006 May 04, 2012 (137)
19 PJP ss292522191 May 09, 2011 (134)
20 ILLUMINA ss481770448 May 04, 2012 (137)
21 ILLUMINA ss484052030 May 04, 2012 (137)
22 ILLUMINA ss534386490 Sep 08, 2015 (146)
23 TISHKOFF ss556349712 Apr 25, 2013 (138)
24 SSMP ss650010832 Apr 25, 2013 (138)
25 ILLUMINA ss779911768 Aug 21, 2014 (142)
26 ILLUMINA ss781564722 Aug 21, 2014 (142)
27 ILLUMINA ss835389798 Aug 21, 2014 (142)
28 EVA-GONL ss978154500 Aug 21, 2014 (142)
29 JMKIDD_LAB ss1070084591 Aug 21, 2014 (142)
30 1000GENOMES ss1302373820 Aug 21, 2014 (142)
31 EVA_GENOME_DK ss1579399139 Apr 01, 2015 (144)
32 EVA_UK10K_ALSPAC ss1606188359 Apr 01, 2015 (144)
33 EVA_UK10K_TWINSUK ss1649182392 Apr 01, 2015 (144)
34 HAMMER_LAB ss1798678030 Sep 08, 2015 (146)
35 WEILL_CORNELL_DGM ss1921405217 Feb 12, 2016 (147)
36 JJLAB ss2021251249 Sep 14, 2016 (149)
37 USC_VALOUEV ss2149319339 Dec 20, 2016 (150)
38 HUMAN_LONGEVITY ss2240647179 Dec 20, 2016 (150)
39 SYSTEMSBIOZJU ss2625125668 Nov 08, 2017 (151)
40 ILLUMINA ss2633764368 Nov 08, 2017 (151)
41 GRF ss2703975289 Nov 08, 2017 (151)
42 GNOMAD ss2788360136 Nov 08, 2017 (151)
43 CSHL ss3344829006 Nov 08, 2017 (151)
44 ILLUMINA ss3628328969 Oct 11, 2018 (152)
45 ILLUMINA ss3631722914 Oct 11, 2018 (152)
46 ILLUMINA ss3642167270 Oct 11, 2018 (152)
47 EVA_DECODE ss3706387188 Jul 13, 2019 (153)
48 ACPOP ss3729535553 Jul 13, 2019 (153)
49 EVA ss3758314886 Jul 13, 2019 (153)
50 PACBIO ss3784203456 Jul 13, 2019 (153)
51 PACBIO ss3789735183 Jul 13, 2019 (153)
52 PACBIO ss3794608823 Jul 13, 2019 (153)
53 KHV_HUMAN_GENOMES ss3802674722 Jul 13, 2019 (153)
54 EVA ss3827602876 Apr 25, 2020 (154)
55 EVA ss3837221632 Apr 25, 2020 (154)
56 EVA ss3842644751 Apr 25, 2020 (154)
57 SGDP_PRJ ss3854987014 Apr 25, 2020 (154)
58 KRGDB ss3900746898 Apr 25, 2020 (154)
59 KOGIC ss3950465116 Apr 25, 2020 (154)
60 TOPMED ss4550738338 Apr 27, 2021 (155)
61 TOMMO_GENOMICS ss5157324526 Apr 27, 2021 (155)
62 1000G_HIGH_COVERAGE ss5252673655 Oct 13, 2022 (156)
63 EVA ss5314823337 Oct 13, 2022 (156)
64 EVA ss5337212550 Oct 13, 2022 (156)
65 HUGCELL_USP ss5452220321 Oct 13, 2022 (156)
66 EVA ss5506853171 Oct 13, 2022 (156)
67 SANFORD_IMAGENETICS ss5631319495 Oct 13, 2022 (156)
68 TOMMO_GENOMICS ss5688458916 Oct 13, 2022 (156)
69 YY_MCH ss5803383144 Oct 13, 2022 (156)
70 EVA ss5821846384 Oct 13, 2022 (156)
71 EVA ss5853030022 Oct 13, 2022 (156)
72 EVA ss5935445160 Oct 13, 2022 (156)
73 EVA ss5957589777 Oct 13, 2022 (156)
74 1000Genomes NC_000002.11 - 242022371 Oct 11, 2018 (152)
75 The Avon Longitudinal Study of Parents and Children NC_000002.11 - 242022371 Oct 11, 2018 (152)
76 The Danish reference pan genome NC_000002.11 - 242022371 Apr 25, 2020 (154)
77 gnomAD - Genomes NC_000002.12 - 241082956 Apr 27, 2021 (155)
78 Genome of the Netherlands Release 5 NC_000002.11 - 242022371 Apr 25, 2020 (154)
79 KOREAN population from KRGDB NC_000002.11 - 242022371 Apr 25, 2020 (154)
80 Korean Genome Project NC_000002.12 - 241082956 Apr 25, 2020 (154)
81 Northern Sweden NC_000002.11 - 242022371 Jul 13, 2019 (153)
82 Qatari NC_000002.11 - 242022371 Apr 25, 2020 (154)
83 SGDP_PRJ NC_000002.11 - 242022371 Apr 25, 2020 (154)
84 Siberian NC_000002.11 - 242022371 Apr 25, 2020 (154)
85 8.3KJPN NC_000002.11 - 242022371 Apr 27, 2021 (155)
86 14KJPN NC_000002.12 - 241082956 Oct 13, 2022 (156)
87 TopMed NC_000002.12 - 241082956 Apr 27, 2021 (155)
88 UK 10K study - Twins NC_000002.11 - 242022371 Oct 11, 2018 (152)
89 A Vietnamese Genetic Variation Database NC_000002.11 - 242022371 Jul 13, 2019 (153)
90 ALFA NC_000002.12 - 241082956 Apr 27, 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)
rs56934470 May 23, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
12339814610 NC_000002.12:241082955:T:A NC_000002.12:241082955:T:A (self)
ss81723329, ss82164069 NC_000002.9:241742360:T:C NC_000002.12:241082955:T:C (self)
ss91608771, ss118150077, ss165809414, ss201979484, ss210524318, ss276967006, ss292522191, ss484052030 NC_000002.10:241671043:T:C NC_000002.12:241082955:T:C (self)
13504805, 7485418, 5564078, 3280858, 7924292, 2820418, 3447147, 7003994, 1835693, 15293833, 7485418, 1626310, ss219918270, ss231661746, ss239104967, ss481770448, ss534386490, ss556349712, ss650010832, ss779911768, ss781564722, ss835389798, ss978154500, ss1070084591, ss1302373820, ss1579399139, ss1606188359, ss1649182392, ss1798678030, ss1921405217, ss2021251249, ss2149319339, ss2625125668, ss2633764368, ss2703975289, ss2788360136, ss3344829006, ss3628328969, ss3631722914, ss3642167270, ss3729535553, ss3758314886, ss3784203456, ss3789735183, ss3794608823, ss3827602876, ss3837221632, ss3854987014, ss3900746898, ss5157324526, ss5314823337, ss5337212550, ss5506853171, ss5631319495, ss5821846384, ss5957589777 NC_000002.11:242022370:T:C NC_000002.12:241082955:T:C (self)
96083822, 6843117, 22296020, 354561217, 12339814610, ss2240647179, ss3706387188, ss3802674722, ss3842644751, ss3950465116, ss4550738338, ss5252673655, ss5452220321, ss5688458916, ss5803383144, ss5853030022, ss5935445160 NC_000002.12:241082955:T:C NC_000002.12:241082955:T:C (self)
ss9953093 NT_005416.10:1192350:T:C NC_000002.12:241082955:T:C (self)
ss14467604 NT_005416.11:1196974:T:C NC_000002.12:241082955:T:C (self)
ss2733695, ss41563131, ss103709655, ss138660795, ss154949609 NT_005416.13:1213238:T:C NC_000002.12:241082955:T:C (self)
12339814610 NC_000002.12:241082955:T:G NC_000002.12:241082955: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 rs1859927

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