Name: rs2725194
Published: September 21, 2022
License: Open Access

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.

rs2725194

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:49170404 (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 / G>C
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.109218 (28909/264690, TOPMED)
A=0.094366 (13222/140114, GnomAD)
A=0.19382 (5477/28258, 14KJPN) (+ 16 more)
A=0.03620 (618/17074, ALFA)
A=0.19379 (3248/16760, 8.3KJPN)
A=0.1729 (1107/6404, 1000G_30x)
A=0.1763 (883/5008, 1000G)
A=0.0819 (367/4480, Estonian)
A=0.0729 (281/3854, ALSPAC)
A=0.0669 (248/3708, TWINSUK)
A=0.2427 (711/2930, KOREAN)
A=0.2249 (412/1832, Korea1K)
A=0.065 (65/998, GoNL)
A=0.110 (66/600, NorthernSweden)
A=0.097 (21/216, Qatari)
G=0.410 (73/178, SGDP_PRJ)
A=0.071 (8/112, HapMap)
A=0.10 (4/40, GENOME_DK)
G=0.33 (4/12, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TMEM273 : 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	17074	G=0.96380	A=0.03620, C=0.00000
European	Sub	13322	G=0.95909	A=0.04091, C=0.00000
African	Sub	2572	G=0.9798	A=0.0202, C=0.0000
African Others	Sub	98	G=1.00	A=0.00, C=0.00
African American	Sub	2474	G=0.9790	A=0.0210, C=0.0000
Asian	Sub	58	G=0.98	A=0.02, C=0.00
East Asian	Sub	42	G=0.98	A=0.02, C=0.00
Other Asian	Sub	16	G=1.00	A=0.00, C=0.00
Latin American 1	Sub	128	G=1.000	A=0.000, C=0.000
Latin American 2	Sub	344	G=1.000	A=0.000, C=0.000
South Asian	Sub	68	G=0.99	A=0.01, C=0.00
Other	Sub	582	G=0.967	A=0.033, C=0.000

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	G=0.890782	A=0.109218
gnomAD - Genomes	Global	Study-wide	140114	G=0.905634	A=0.094366
gnomAD - Genomes	European	Sub	75886	G=0.92860	A=0.07140
gnomAD - Genomes	African	Sub	41980	G=0.91715	A=0.08285
gnomAD - Genomes	American	Sub	13640	G=0.79003	A=0.20997
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	G=0.9064	A=0.0936
gnomAD - Genomes	East Asian	Sub	3132	G=0.7011	A=0.2989
gnomAD - Genomes	Other	Sub	2152	G=0.9001	A=0.0999
14KJPN	JAPANESE	Study-wide	28258	G=0.80618	A=0.19382
Allele Frequency Aggregator	Total	Global	17074	G=0.96380	A=0.03620, C=0.00000
Allele Frequency Aggregator	European	Sub	13322	G=0.95909	A=0.04091, C=0.00000
Allele Frequency Aggregator	African	Sub	2572	G=0.9798	A=0.0202, C=0.0000
Allele Frequency Aggregator	Other	Sub	582	G=0.967	A=0.033, C=0.000
Allele Frequency Aggregator	Latin American 2	Sub	344	G=1.000	A=0.000, C=0.000
Allele Frequency Aggregator	Latin American 1	Sub	128	G=1.000	A=0.000, C=0.000
Allele Frequency Aggregator	South Asian	Sub	68	G=0.99	A=0.01, C=0.00
Allele Frequency Aggregator	Asian	Sub	58	G=0.98	A=0.02, C=0.00
8.3KJPN	JAPANESE	Study-wide	16760	G=0.80621	A=0.19379
1000Genomes_30x	Global	Study-wide	6404	G=0.8271	A=0.1729
1000Genomes_30x	African	Sub	1786	G=0.9239	A=0.0761
1000Genomes_30x	Europe	Sub	1266	G=0.9234	A=0.0766
1000Genomes_30x	South Asian	Sub	1202	G=0.7579	A=0.2421
1000Genomes_30x	East Asian	Sub	1170	G=0.6726	A=0.3274
1000Genomes_30x	American	Sub	980	G=0.796	A=0.204
1000Genomes	Global	Study-wide	5008	G=0.8237	A=0.1763
1000Genomes	African	Sub	1322	G=0.9221	A=0.0779
1000Genomes	East Asian	Sub	1008	G=0.6796	A=0.3204
1000Genomes	Europe	Sub	1006	G=0.9225	A=0.0775
1000Genomes	South Asian	Sub	978	G=0.760	A=0.240
1000Genomes	American	Sub	694	G=0.793	A=0.207
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.9181	A=0.0819
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.9271	A=0.0729
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.9331	A=0.0669
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.7573	A=0.2427
Korean Genome Project	KOREAN	Study-wide	1832	G=0.7751	A=0.2249
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.935	A=0.065
Northern Sweden	ACPOP	Study-wide	600	G=0.890	A=0.110
Qatari	Global	Study-wide	216	G=0.903	A=0.097
SGDP_PRJ	Global	Study-wide	178	G=0.410	A=0.590
HapMap	Global	Study-wide	112	G=0.929	A=0.071
HapMap	African	Sub	112	G=0.929	A=0.071
The Danish reference pan genome	Danish	Study-wide	40	G=0.90	A=0.10
Siberian	Global	Study-wide	12	G=0.33	A=0.67

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 10	NC_000010.11:g.49170404G>A
GRCh38.p14 chr 10	NC_000010.11:g.49170404G>C
GRCh37.p13 chr 10	NC_000010.10:g.50378449G>A
GRCh37.p13 chr 10	NC_000010.10:g.50378449G>C

Gene: TMEM273, transmembrane protein 273 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TMEM273 transcript variant 1	NM_001010863.4:c.44-2442C… NM_001010863.4:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant 2	NM_001288740.3:c.44-2442C… NM_001288740.3:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant 3	NM_001288741.3:c.44-2442C… NM_001288741.3:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant 4	NM_001288742.3:c.44-2442C… NM_001288742.3:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant 5	NM_001288743.3:c.44-2442C… NM_001288743.3:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant 6	NM_001353330.2:c.44-2442C… NM_001353330.2:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant 7	NM_001353331.2:c.44-2442C… NM_001353331.2:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X2	XM_011539378.3:c.44-2442C… XM_011539378.3:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X12	XM_011539379.2:c.44-2442C… XM_011539379.2:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X5	XM_011539382.2:c.44-2442C… XM_011539382.2:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X14	XM_011539384.2:c.44-2442C… XM_011539384.2:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X15	XM_011539385.2:c.44-2442C… XM_011539385.2:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X1	XM_017015792.2:c.44-2442C… XM_017015792.2:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X3	XM_017015793.2:c.44-2442C… XM_017015793.2:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X8	XM_017015794.2:c.44-2442C… XM_017015794.2:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X9	XM_017015796.2:c.44-2442C… XM_017015796.2:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X10	XM_017015797.2:c.44-2442C… XM_017015797.2:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X11	XM_024447853.2:c.44-2442C… XM_024447853.2:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X4	XM_047424684.1:c.44-2442C… XM_047424684.1:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X13	XM_047424685.1:c.44-2442C… XM_047424685.1:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X6	XM_047424686.1:c.44-2442C… XM_047424686.1:c.44-2442C>T	N/A	Intron Variant
TMEM273 transcript variant X7	XM_047424687.1:c.44-2442C… XM_047424687.1:c.44-2442C>T	N/A	Intron Variant

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

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	C
GRCh38.p14 chr 10	NC_000010.11:g.49170404=	NC_000010.11:g.49170404G>A	NC_000010.11:g.49170404G>C
GRCh37.p13 chr 10	NC_000010.10:g.50378449=	NC_000010.10:g.50378449G>A	NC_000010.10:g.50378449G>C
C10orf128 transcript	NM_001010863.1:c.44-2442=	NM_001010863.1:c.44-2442C>T	NM_001010863.1:c.44-2442C>G
TMEM273 transcript variant 1	NM_001010863.4:c.44-2442=	NM_001010863.4:c.44-2442C>T	NM_001010863.4:c.44-2442C>G
TMEM273 transcript variant 2	NM_001288740.3:c.44-2442=	NM_001288740.3:c.44-2442C>T	NM_001288740.3:c.44-2442C>G
TMEM273 transcript variant 3	NM_001288741.3:c.44-2442=	NM_001288741.3:c.44-2442C>T	NM_001288741.3:c.44-2442C>G
TMEM273 transcript variant 4	NM_001288742.3:c.44-2442=	NM_001288742.3:c.44-2442C>T	NM_001288742.3:c.44-2442C>G
TMEM273 transcript variant 5	NM_001288743.3:c.44-2442=	NM_001288743.3:c.44-2442C>T	NM_001288743.3:c.44-2442C>G
TMEM273 transcript variant 6	NM_001353330.2:c.44-2442=	NM_001353330.2:c.44-2442C>T	NM_001353330.2:c.44-2442C>G
TMEM273 transcript variant 7	NM_001353331.2:c.44-2442=	NM_001353331.2:c.44-2442C>T	NM_001353331.2:c.44-2442C>G
C10orf128 transcript variant X1	XM_005269586.1:c.44-2442=	XM_005269586.1:c.44-2442C>T	XM_005269586.1:c.44-2442C>G
TMEM273 transcript variant X2	XM_011539378.3:c.44-2442=	XM_011539378.3:c.44-2442C>T	XM_011539378.3:c.44-2442C>G
TMEM273 transcript variant X12	XM_011539379.2:c.44-2442=	XM_011539379.2:c.44-2442C>T	XM_011539379.2:c.44-2442C>G
TMEM273 transcript variant X5	XM_011539382.2:c.44-2442=	XM_011539382.2:c.44-2442C>T	XM_011539382.2:c.44-2442C>G
TMEM273 transcript variant X14	XM_011539384.2:c.44-2442=	XM_011539384.2:c.44-2442C>T	XM_011539384.2:c.44-2442C>G
TMEM273 transcript variant X15	XM_011539385.2:c.44-2442=	XM_011539385.2:c.44-2442C>T	XM_011539385.2:c.44-2442C>G
TMEM273 transcript variant X1	XM_017015792.2:c.44-2442=	XM_017015792.2:c.44-2442C>T	XM_017015792.2:c.44-2442C>G
TMEM273 transcript variant X3	XM_017015793.2:c.44-2442=	XM_017015793.2:c.44-2442C>T	XM_017015793.2:c.44-2442C>G
TMEM273 transcript variant X8	XM_017015794.2:c.44-2442=	XM_017015794.2:c.44-2442C>T	XM_017015794.2:c.44-2442C>G
TMEM273 transcript variant X9	XM_017015796.2:c.44-2442=	XM_017015796.2:c.44-2442C>T	XM_017015796.2:c.44-2442C>G
TMEM273 transcript variant X10	XM_017015797.2:c.44-2442=	XM_017015797.2:c.44-2442C>T	XM_017015797.2:c.44-2442C>G
TMEM273 transcript variant X11	XM_024447853.2:c.44-2442=	XM_024447853.2:c.44-2442C>T	XM_024447853.2:c.44-2442C>G
TMEM273 transcript variant X4	XM_047424684.1:c.44-2442=	XM_047424684.1:c.44-2442C>T	XM_047424684.1:c.44-2442C>G
TMEM273 transcript variant X13	XM_047424685.1:c.44-2442=	XM_047424685.1:c.44-2442C>T	XM_047424685.1:c.44-2442C>G
TMEM273 transcript variant X6	XM_047424686.1:c.44-2442=	XM_047424686.1:c.44-2442C>T	XM_047424686.1:c.44-2442C>G
TMEM273 transcript variant X7	XM_047424687.1:c.44-2442=	XM_047424687.1:c.44-2442C>T	XM_047424687.1:c.44-2442C>G

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, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss3848182	Sep 28, 2001 (100)
2	SC_SNP	ss12971572	Dec 05, 2003 (119)
3	SSAHASNP	ss20734433	Apr 05, 2004 (121)
4	ABI	ss43535945	Mar 15, 2006 (126)
5	HGSV	ss82707088	Dec 16, 2007 (130)
6	HUMANGENOME_JCVI	ss97646720	Feb 06, 2009 (130)
7	GMI	ss154980579	Dec 01, 2009 (131)
8	BCM-HGSC-SUB	ss207422982	Jul 04, 2010 (132)
9	1000GENOMES	ss224707618	Jul 14, 2010 (132)
10	1000GENOMES	ss235162716	Jul 15, 2010 (132)
11	1000GENOMES	ss241871833	Jul 15, 2010 (132)
12	GMI	ss280604055	May 04, 2012 (137)
13	TISHKOFF	ss561937895	Apr 25, 2013 (138)
14	SSMP	ss656678396	Apr 25, 2013 (138)
15	EVA-GONL	ss987458656	Aug 21, 2014 (142)
16	JMKIDD_LAB	ss1076961752	Aug 21, 2014 (142)
17	1000GENOMES	ss1337331544	Aug 21, 2014 (142)
18	DDI	ss1426310057	Apr 01, 2015 (144)
19	EVA_GENOME_DK	ss1575093758	Apr 01, 2015 (144)
20	EVA_DECODE	ss1597122556	Apr 01, 2015 (144)
21	EVA_UK10K_ALSPAC	ss1624515075	Apr 01, 2015 (144)
22	EVA_UK10K_TWINSUK	ss1667509108	Apr 01, 2015 (144)
23	WEILL_CORNELL_DGM	ss1930816276	Feb 12, 2016 (147)
24	GENOMED	ss1967119542	Jul 19, 2016 (147)
25	JJLAB	ss2026130032	Sep 14, 2016 (149)
26	USC_VALOUEV	ss2154404182	Dec 20, 2016 (150)
27	HUMAN_LONGEVITY	ss2174566790	Dec 20, 2016 (150)
28	SYSTEMSBIOZJU	ss2627535188	Nov 08, 2017 (151)
29	GRF	ss2698644043	Nov 08, 2017 (151)
30	GNOMAD	ss2888479722	Nov 08, 2017 (151)
31	SWEGEN	ss3006429635	Nov 08, 2017 (151)
32	BIOINF_KMB_FNS_UNIBA	ss3026853911	Nov 08, 2017 (151)
33	CSHL	ss3349106208	Nov 08, 2017 (151)
34	URBANLAB	ss3649362068	Oct 12, 2018 (152)
35	EGCUT_WGS	ss3673849175	Jul 13, 2019 (153)
36	EVA_DECODE	ss3689828581	Jul 13, 2019 (153)
37	ACPOP	ss3737294990	Jul 13, 2019 (153)
38	EVA	ss3748070704	Jul 13, 2019 (153)
39	KHV_HUMAN_GENOMES	ss3813442643	Jul 13, 2019 (153)
40	EVA	ss3832107800	Apr 26, 2020 (154)
41	SGDP_PRJ	ss3874143240	Apr 26, 2020 (154)
42	KRGDB	ss3922203899	Apr 26, 2020 (154)
43	KOGIC	ss3967836927	Apr 26, 2020 (154)
44	TOPMED	ss4851537268	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5197513700	Apr 26, 2021 (155)
46	1000G_HIGH_COVERAGE	ss5283948637	Oct 16, 2022 (156)
47	EVA	ss5393291673	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5479544407	Oct 16, 2022 (156)
49	EVA	ss5510001461	Oct 16, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5577840693	Oct 16, 2022 (156)
51	SANFORD_IMAGENETICS	ss5649225565	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5743321401	Oct 16, 2022 (156)
53	YY_MCH	ss5811505604	Oct 16, 2022 (156)
54	EVA	ss5824355995	Oct 16, 2022 (156)
55	EVA	ss5849552233	Oct 16, 2022 (156)
56	EVA	ss5878801252	Oct 16, 2022 (156)
57	EVA	ss5940495609	Oct 16, 2022 (156)
58	1000Genomes	NC_000010.10 - 50378449	Oct 12, 2018 (152)
59	1000Genomes_30x	NC_000010.11 - 49170404	Oct 16, 2022 (156)
60	The Avon Longitudinal Study of Parents and Children	NC_000010.10 - 50378449	Oct 12, 2018 (152)
61	Genetic variation in the Estonian population	NC_000010.10 - 50378449	Oct 12, 2018 (152)
62	The Danish reference pan genome	NC_000010.10 - 50378449	Apr 26, 2020 (154)
63	gnomAD - Genomes	NC_000010.11 - 49170404	Apr 26, 2021 (155)
64	Genome of the Netherlands Release 5	NC_000010.10 - 50378449	Apr 26, 2020 (154)
65	HapMap	NC_000010.11 - 49170404	Apr 26, 2020 (154)
66	KOREAN population from KRGDB	NC_000010.10 - 50378449	Apr 26, 2020 (154)
67	Korean Genome Project	NC_000010.11 - 49170404	Apr 26, 2020 (154)
68	Northern Sweden	NC_000010.10 - 50378449	Jul 13, 2019 (153)
69	Qatari	NC_000010.10 - 50378449	Apr 26, 2020 (154)
70	SGDP_PRJ	NC_000010.10 - 50378449	Apr 26, 2020 (154)
71	Siberian	NC_000010.10 - 50378449	Apr 26, 2020 (154)
72	8.3KJPN	NC_000010.10 - 50378449	Apr 26, 2021 (155)
73	14KJPN	NC_000010.11 - 49170404	Oct 16, 2022 (156)
74	TopMed	NC_000010.11 - 49170404	Apr 26, 2021 (155)
75	UK 10K study - Twins	NC_000010.10 - 50378449	Oct 12, 2018 (152)
76	ALFA	NC_000010.11 - 49170404	Apr 26, 2021 (155)

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)
rs61320191	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss82707088	NC_000010.8:50048454:G:A	NC_000010.11:49170403:G:A	(self)
ss207422982, ss280604055, ss1597122556	NC_000010.9:50048454:G:A	NC_000010.11:49170403:G:A	(self)
49714759, 27596645, 19587423, 2142747, 12303556, 29381293, 10579855, 12858206, 26160220, 6920536, 55483007, 27596645, ss224707618, ss235162716, ss241871833, ss561937895, ss656678396, ss987458656, ss1076961752, ss1337331544, ss1426310057, ss1575093758, ss1624515075, ss1667509108, ss1930816276, ss1967119542, ss2026130032, ss2154404182, ss2627535188, ss2698644043, ss2888479722, ss3006429635, ss3349106208, ss3673849175, ss3737294990, ss3748070704, ss3832107800, ss3874143240, ss3922203899, ss5197513700, ss5393291673, ss5510001461, ss5649225565, ss5824355995, ss5940495609	NC_000010.10:50378448:G:A	NC_000010.11:49170403:G:A	(self)
65366628, 351483337, 394643, 24214928, 77158505, 67082923, 2359937422, ss2174566790, ss3026853911, ss3649362068, ss3689828581, ss3813442643, ss3967836927, ss4851537268, ss5283948637, ss5479544407, ss5577840693, ss5743321401, ss5811505604, ss5849552233, ss5878801252	NC_000010.11:49170403:G:A	NC_000010.11:49170403:G:A	(self)
ss12971572, ss20734433	NT_017696.14:1182912:G:A	NC_000010.11:49170403:G:A	(self)
ss3848182, ss43535945, ss97646720, ss154980579	NT_030059.13:1182912:G:A	NC_000010.11:49170403:G:A	(self)
2359937422	NC_000010.11:49170403:G:C	NC_000010.11:49170403:G:C	(self)

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

No publications for rs2725194

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs2725194