Name: rs2241107
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.

rs2241107

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:156212919 (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>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.426801 (112970/264690, TOPMED)
C=0.431283 (60396/140038, GnomAD)
C=0.17704 (5002/28254, 14KJPN) (+ 17 more)
C=0.29032 (5238/18042, ALFA)
C=0.17651 (2958/16758, 8.3KJPN)
C=0.3943 (2525/6404, 1000G_30x)
C=0.3818 (1912/5008, 1000G)
C=0.4156 (1862/4480, Estonian)
C=0.3544 (1366/3854, ALSPAC)
C=0.3714 (1377/3708, TWINSUK)
C=0.1536 (450/2930, KOREAN)
C=0.4134 (778/1882, HapMap)
C=0.1632 (299/1832, Korea1K)
C=0.278 (174/626, Chileans)
C=0.343 (206/600, NorthernSweden)
T=0.366 (98/268, SGDP_PRJ)
C=0.370 (80/216, Qatari)
C=0.103 (22/214, Vietnamese)
C=0.33 (13/40, GENOME_DK)
T=0.36 (10/28, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PMF1 : 2KB Upstream Variant
PMF1-BGLAP : 2KB Upstream Variant
SLC25A44 : 500B Downstream 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	18042	T=0.70968	C=0.29032, G=0.00000
European	Sub	13030	T=0.71765	C=0.28235, G=0.00000
African	Sub	1230	T=0.5797	C=0.4203, G=0.0000
African Others	Sub	32	T=0.59	C=0.41, G=0.00
African American	Sub	1198	T=0.5793	C=0.4207, G=0.0000
Asian	Sub	136	T=0.926	C=0.074, G=0.000
East Asian	Sub	90	T=0.97	C=0.03, G=0.00
Other Asian	Sub	46	T=0.85	C=0.15, G=0.00
Latin American 1	Sub	172	T=0.610	C=0.390, G=0.000
Latin American 2	Sub	2386	T=0.7246	C=0.2754, G=0.0000
South Asian	Sub	66	T=0.89	C=0.11, G=0.00
Other	Sub	1022	T=0.7055	C=0.2945, G=0.0000

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	T=0.573199	C=0.426801
gnomAD - Genomes	Global	Study-wide	140038	T=0.568717	C=0.431283
gnomAD - Genomes	European	Sub	75830	T=0.64415	C=0.35585
gnomAD - Genomes	African	Sub	41968	T=0.37059	C=0.62941
gnomAD - Genomes	American	Sub	13648	T=0.66317	C=0.33683
gnomAD - Genomes	Ashkenazi Jewish	Sub	3316	T=0.7014	C=0.2986
gnomAD - Genomes	East Asian	Sub	3126	T=0.8353	C=0.1647
gnomAD - Genomes	Other	Sub	2150	T=0.5837	C=0.4163
14KJPN	JAPANESE	Study-wide	28254	T=0.82296	C=0.17704
Allele Frequency Aggregator	Total	Global	18042	T=0.70968	C=0.29032, G=0.00000
Allele Frequency Aggregator	European	Sub	13030	T=0.71765	C=0.28235, G=0.00000
Allele Frequency Aggregator	Latin American 2	Sub	2386	T=0.7246	C=0.2754, G=0.0000
Allele Frequency Aggregator	African	Sub	1230	T=0.5797	C=0.4203, G=0.0000
Allele Frequency Aggregator	Other	Sub	1022	T=0.7055	C=0.2945, G=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	172	T=0.610	C=0.390, G=0.000
Allele Frequency Aggregator	Asian	Sub	136	T=0.926	C=0.074, G=0.000
Allele Frequency Aggregator	South Asian	Sub	66	T=0.89	C=0.11, G=0.00
8.3KJPN	JAPANESE	Study-wide	16758	T=0.82349	C=0.17651
1000Genomes_30x	Global	Study-wide	6404	T=0.6057	C=0.3943
1000Genomes_30x	African	Sub	1786	T=0.3214	C=0.6786
1000Genomes_30x	Europe	Sub	1266	T=0.6445	C=0.3555
1000Genomes_30x	South Asian	Sub	1202	T=0.6930	C=0.3070
1000Genomes_30x	East Asian	Sub	1170	T=0.8513	C=0.1487
1000Genomes_30x	American	Sub	980	T=0.673	C=0.327
1000Genomes	Global	Study-wide	5008	T=0.6182	C=0.3818
1000Genomes	African	Sub	1322	T=0.3275	C=0.6725
1000Genomes	East Asian	Sub	1008	T=0.8621	C=0.1379
1000Genomes	Europe	Sub	1006	T=0.6382	C=0.3618
1000Genomes	South Asian	Sub	978	T=0.700	C=0.300
1000Genomes	American	Sub	694	T=0.673	C=0.327
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.5844	C=0.4156
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.6456	C=0.3544
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.6286	C=0.3714
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.8464	C=0.1536, G=0.0000
HapMap	Global	Study-wide	1882	T=0.5866	C=0.4134
HapMap	American	Sub	768	T=0.667	C=0.333
HapMap	African	Sub	690	T=0.371	C=0.629
HapMap	Asian	Sub	254	T=0.862	C=0.138
HapMap	Europe	Sub	170	T=0.688	C=0.312
Korean Genome Project	KOREAN	Study-wide	1832	T=0.8368	C=0.1632
Chileans	Chilean	Study-wide	626	T=0.722	C=0.278
Northern Sweden	ACPOP	Study-wide	600	T=0.657	C=0.343
SGDP_PRJ	Global	Study-wide	268	T=0.366	C=0.634
Qatari	Global	Study-wide	216	T=0.630	C=0.370
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.897	C=0.103
The Danish reference pan genome	Danish	Study-wide	40	T=0.68	C=0.33
Siberian	Global	Study-wide	28	T=0.36	C=0.64

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 1	NC_000001.11:g.156212919T>C
GRCh38.p14 chr 1	NC_000001.11:g.156212919T>G
GRCh37.p13 chr 1	NC_000001.10:g.156182710T>C
GRCh37.p13 chr 1	NC_000001.10:g.156182710T>G

Gene: PMF1, polyamine modulated factor 1 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
PMF1 transcript variant 3	NM_001199653.2:c.	N/A	Upstream Transcript Variant
PMF1 transcript variant 1	NM_001199654.2:c.	N/A	Upstream Transcript Variant
PMF1 transcript variant 4	NM_001393909.1:c.	N/A	Upstream Transcript Variant
PMF1 transcript variant 5	NM_001393910.1:c.	N/A	Upstream Transcript Variant
PMF1 transcript variant 6	NM_001393911.1:c.	N/A	Upstream Transcript Variant
PMF1 transcript variant 7	NM_001393912.1:c.	N/A	Upstream Transcript Variant
PMF1 transcript variant 8	NM_001393913.1:c.	N/A	Upstream Transcript Variant
PMF1 transcript variant 9	NM_001393914.1:c.	N/A	Upstream Transcript Variant
PMF1 transcript variant 10	NM_001393915.1:c.	N/A	Upstream Transcript Variant
PMF1 transcript variant 2	NM_007221.4:c.	N/A	Upstream Transcript Variant

Gene: PMF1-BGLAP, PMF1-BGLAP readthrough (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
PMF1-BGLAP transcript variant 1	NM_001199661.1:c.	N/A	Upstream Transcript Variant
PMF1-BGLAP transcript variant 2	NM_001199662.1:c.	N/A	Upstream Transcript Variant
PMF1-BGLAP transcript variant 3	NM_001199663.1:c.	N/A	Upstream Transcript Variant
PMF1-BGLAP transcript variant 4	NM_001199664.1:c.	N/A	Upstream Transcript Variant

Gene: SLC25A44, solute carrier family 25 member 44 (plus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
SLC25A44 transcript variant 1	NM_001286184.2:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant 6	NM_001377385.1:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant 7	NM_001377386.1:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant 8	NM_001377387.1:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant 9	NM_001377388.1:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant 10	NM_001377389.1:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant 11	NM_001377390.1:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant 2	NM_014655.4:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant 5	NR_104408.2:n.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant 3	NR_104411.2:n.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant 4	NR_104412.2:n.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant X1	XM_011510180.2:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant X2	XM_011510181.3:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant X3	XM_047435097.1:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant X4	XM_047435098.1:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant X5	XM_047435101.1:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant X6	XM_047435102.1:c.	N/A	Downstream Transcript Variant
SLC25A44 transcript variant X7	XM_047435103.1:c.	N/A	Downstream Transcript 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	T=	C	G
GRCh38.p14 chr 1	NC_000001.11:g.156212919=	NC_000001.11:g.156212919T>C	NC_000001.11:g.156212919T>G
GRCh37.p13 chr 1	NC_000001.10:g.156182710=	NC_000001.10:g.156182710T>C	NC_000001.10:g.156182710T>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#.

81 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	YUSUKE	ss3196942	Aug 15, 2001 (98)
2	SC_JCM	ss3560505	Sep 28, 2001 (100)
3	BCM_SSAHASNP	ss9834843	Jul 11, 2003 (116)
4	WI_SSAHASNP	ss11365925	Jul 11, 2003 (116)
5	CSHL-HAPMAP	ss17326416	Feb 27, 2004 (120)
6	ABI	ss43906769	Mar 14, 2006 (126)
7	AFFY	ss66046146	Nov 29, 2006 (127)
8	AFFY	ss75945905	Dec 08, 2007 (130)
9	SI_EXO	ss76892496	Dec 06, 2007 (129)
10	KRIBB_YJKIM	ss81734369	Dec 14, 2007 (130)
11	HGSV	ss83283225	Dec 15, 2007 (130)
12	HGSV	ss85348679	Dec 15, 2007 (130)
13	1000GENOMES	ss108605073	Jan 23, 2009 (130)
14	1000GENOMES	ss111166924	Jan 25, 2009 (130)
15	ILLUMINA-UK	ss119036037	Feb 15, 2009 (130)
16	ENSEMBL	ss161176843	Dec 01, 2009 (131)
17	COMPLETE_GENOMICS	ss164138123	Jul 04, 2010 (132)
18	COMPLETE_GENOMICS	ss165235201	Jul 04, 2010 (132)
19	COMPLETE_GENOMICS	ss167141682	Jul 04, 2010 (132)
20	AFFY	ss169499903	Jul 04, 2010 (132)
21	BUSHMAN	ss199096635	Jul 04, 2010 (132)
22	1000GENOMES	ss218654918	Jul 14, 2010 (132)
23	1000GENOMES	ss230734627	Jul 14, 2010 (132)
24	1000GENOMES	ss238381665	Jul 15, 2010 (132)
25	BL	ss253514944	May 09, 2011 (134)
26	GMI	ss276053917	May 04, 2012 (137)
27	PJP	ss290638546	May 09, 2011 (134)
28	SSMP	ss648419539	Apr 25, 2013 (138)
29	EVA-GONL	ss975691994	Aug 21, 2014 (142)
30	JMKIDD_LAB	ss1068275116	Aug 21, 2014 (142)
31	1000GENOMES	ss1292965732	Aug 21, 2014 (142)
32	DDI	ss1425980775	Apr 01, 2015 (144)
33	EVA_GENOME_DK	ss1574396547	Apr 01, 2015 (144)
34	EVA_DECODE	ss1585073811	Apr 01, 2015 (144)
35	EVA_UK10K_ALSPAC	ss1601234144	Apr 01, 2015 (144)
36	EVA_UK10K_TWINSUK	ss1644228177	Apr 01, 2015 (144)
37	EVA_SVP	ss1712371597	Apr 01, 2015 (144)
38	HAMMER_LAB	ss1795103403	Sep 08, 2015 (146)
39	WEILL_CORNELL_DGM	ss1918925531	Feb 12, 2016 (147)
40	JJLAB	ss2019977802	Sep 14, 2016 (149)
41	USC_VALOUEV	ss2148003408	Dec 20, 2016 (150)
42	HUMAN_LONGEVITY	ss2166626114	Dec 20, 2016 (150)
43	SYSTEMSBIOZJU	ss2624496730	Nov 08, 2017 (151)
44	GRF	ss2697976004	Nov 08, 2017 (151)
45	GNOMAD	ss2761443047	Nov 08, 2017 (151)
46	SWEGEN	ss2987769152	Nov 08, 2017 (151)
47	CSHL	ss3343714216	Nov 08, 2017 (151)
48	EGCUT_WGS	ss3655708270	Jul 12, 2019 (153)
49	EVA_DECODE	ss3687802631	Jul 12, 2019 (153)
50	ACPOP	ss3727493086	Jul 12, 2019 (153)
51	EVA	ss3746819409	Jul 12, 2019 (153)
52	KHV_HUMAN_GENOMES	ss3799819407	Jul 12, 2019 (153)
53	EVA	ss3826428261	Apr 25, 2020 (154)
54	EVA	ss3836608667	Apr 25, 2020 (154)
55	EVA	ss3842017945	Apr 25, 2020 (154)
56	SGDP_PRJ	ss3850025723	Apr 25, 2020 (154)
57	KRGDB	ss3895240563	Apr 25, 2020 (154)
58	KOGIC	ss3945674872	Apr 25, 2020 (154)
59	FSA-LAB	ss3983948120	Apr 25, 2021 (155)
60	FSA-LAB	ss3983948121	Apr 25, 2021 (155)
61	EVA	ss3986140388	Apr 25, 2021 (155)
62	TOPMED	ss4468689947	Apr 25, 2021 (155)
63	EVA	ss5141879776	Apr 25, 2021 (155)
64	TOMMO_GENOMICS	ss5146536605	Apr 25, 2021 (155)
65	EVA	ss5237164098	Apr 25, 2021 (155)
66	1000G_HIGH_COVERAGE	ss5244328776	Oct 12, 2022 (156)
67	EVA	ss5322116449	Oct 12, 2022 (156)
68	HUGCELL_USP	ss5444917560	Oct 12, 2022 (156)
69	EVA	ss5506031953	Oct 12, 2022 (156)
70	1000G_HIGH_COVERAGE	ss5517675161	Oct 12, 2022 (156)
71	EVA	ss5623916664	Oct 12, 2022 (156)
72	EVA	ss5623998069	Oct 12, 2022 (156)
73	SANFORD_IMAGENETICS	ss5626609870	Oct 12, 2022 (156)
74	TOMMO_GENOMICS	ss5673751146	Oct 12, 2022 (156)
75	YY_MCH	ss5801267896	Oct 12, 2022 (156)
76	EVA	ss5832678449	Oct 12, 2022 (156)
77	EVA	ss5848273564	Oct 12, 2022 (156)
78	EVA	ss5849111719	Oct 12, 2022 (156)
79	EVA	ss5910284578	Oct 12, 2022 (156)
80	EVA	ss5938404146	Oct 12, 2022 (156)
81	EVA	ss5979990673	Oct 12, 2022 (156)
82	1000Genomes	NC_000001.10 - 156182710	Oct 11, 2018 (152)
83	1000Genomes_30x	NC_000001.11 - 156212919	Oct 12, 2022 (156)
84	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 156182710	Oct 11, 2018 (152)
85	Chileans	NC_000001.10 - 156182710	Apr 25, 2020 (154)
86	Genetic variation in the Estonian population	NC_000001.10 - 156182710	Oct 11, 2018 (152)
87	The Danish reference pan genome	NC_000001.10 - 156182710	Apr 25, 2020 (154)
88	gnomAD - Genomes	NC_000001.11 - 156212919	Apr 25, 2021 (155)
89	HapMap	NC_000001.11 - 156212919	Apr 25, 2020 (154)
90	KOREAN population from KRGDB	NC_000001.10 - 156182710	Apr 25, 2020 (154)
91	Korean Genome Project	NC_000001.11 - 156212919	Apr 25, 2020 (154)
92	Northern Sweden	NC_000001.10 - 156182710	Jul 12, 2019 (153)
93	Qatari	NC_000001.10 - 156182710	Apr 25, 2020 (154)
94	SGDP_PRJ	NC_000001.10 - 156182710	Apr 25, 2020 (154)
95	Siberian	NC_000001.10 - 156182710	Apr 25, 2020 (154)
96	8.3KJPN	NC_000001.10 - 156182710	Apr 25, 2021 (155)
97	14KJPN	NC_000001.11 - 156212919	Oct 12, 2022 (156)
98	TopMed	NC_000001.11 - 156212919	Apr 25, 2021 (155)
99	UK 10K study - Twins	NC_000001.10 - 156182710	Oct 11, 2018 (152)
100	A Vietnamese Genetic Variation Database	NC_000001.10 - 156182710	Jul 12, 2019 (153)
101	ALFA	NC_000001.11 - 156212919	Apr 25, 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)
rs56447417	May 25, 2008 (130)
rs57033182	Feb 27, 2009 (130)
rs59530981	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss83283225, ss85348679	NC_000001.8:152995782:T:C	NC_000001.11:156212918:T:C	(self)
ss66046146, ss75945905, ss108605073, ss111166924, ss119036037, ss164138123, ss165235201, ss167141682, ss169499903, ss199096635, ss253514944, ss276053917, ss290638546, ss1585073811, ss1712371597	NC_000001.9:154449333:T:C	NC_000001.11:156212918:T:C	(self)
3759170, 2043625, 21175, 1446518, 1711442, 2417957, 777951, 967461, 2042703, 519762, 4505912, 2043625, 437886, ss218654918, ss230734627, ss238381665, ss648419539, ss975691994, ss1068275116, ss1292965732, ss1425980775, ss1574396547, ss1601234144, ss1644228177, ss1795103403, ss1918925531, ss2019977802, ss2148003408, ss2624496730, ss2697976004, ss2761443047, ss2987769152, ss3343714216, ss3655708270, ss3727493086, ss3746819409, ss3826428261, ss3836608667, ss3850025723, ss3895240563, ss3983948120, ss3983948121, ss3986140388, ss5146536605, ss5322116449, ss5506031953, ss5623916664, ss5623998069, ss5626609870, ss5832678449, ss5848273564, ss5938404146, ss5979990673	NC_000001.10:156182709:T:C	NC_000001.11:156212918:T:C	(self)
5201096, 27378883, 177983, 2052873, 7588250, 32296282, 5843784649, ss2166626114, ss3687802631, ss3799819407, ss3842017945, ss3945674872, ss4468689947, ss5141879776, ss5237164098, ss5244328776, ss5444917560, ss5517675161, ss5673751146, ss5801267896, ss5849111719, ss5910284578	NC_000001.11:156212918:T:C	NC_000001.11:156212918:T:C	(self)
ss76892496	NT_004487.18:6673064:T:C	NC_000001.11:156212918:T:C	(self)
ss3196942, ss3560505, ss43906769, ss81734369, ss161176843	NT_004487.19:7671351:T:C	NC_000001.11:156212918:T:C	(self)
ss9834843, ss11365925	NT_004668.15:2635110:T:C	NC_000001.11:156212918:T:C	(self)
ss17326416	NT_079484.1:2632541:T:C	NC_000001.11:156212918:T:C	(self)
2417957, ss3895240563	NC_000001.10:156182709:T:G	NC_000001.11:156212918:T:G	(self)
5843784649	NC_000001.11:156212918:T:G	NC_000001.11:156212918:T:G	(self)

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

1 citation for rs2241107

PMID	Title	Author	Year	Journal
15637659	Linkage disequilibrium patterns and tagSNP transferability among European populations.	Mueller JC et al.	2005	American journal of human genetics

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
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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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs2241107