Name: rs925255
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.

rs925255

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:28391927 (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: C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: T=0.369787 (97879/264690, TOPMED)
T=0.435648 (86403/198332, ALFA)
T=0.380796 (51773/135960, GnomAD) (+ 18 more)
T=0.30240 (23797/78694, PAGE_STUDY)
T=0.23238 (6566/28256, 14KJPN)
T=0.22893 (3836/16756, 8.3KJPN)
T=0.3442 (2204/6404, 1000G_30x)
T=0.3425 (1715/5008, 1000G)
T=0.4279 (1905/4452, Estonian)
T=0.4683 (1805/3854, ALSPAC)
T=0.4657 (1727/3708, TWINSUK)
T=0.1918 (559/2914, KOREAN)
T=0.3205 (668/2084, HGDP_Stanford)
T=0.3145 (595/1892, HapMap)
T=0.246 (194/790, PRJEB37584)
T=0.495 (296/598, NorthernSweden)
C=0.374 (104/278, SGDP_PRJ)
T=0.255 (55/216, Qatari)
T=0.45 (18/40, GENOME_DK)
C=0.45 (18/40, Ancient Sardinia)
C=0.22 (8/36, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FOSL2-AS1 : Intron Variant
FOSL2 : 2KB Upstream Variant
Publications: 5 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	198332	C=0.564352	G=0.000000, T=0.435648
European	Sub	172192	C=0.553191	G=0.000000, T=0.446809
African	Sub	9914	C=0.7262	G=0.0000, T=0.2738
African Others	Sub	340	C=0.741	G=0.000, T=0.259
African American	Sub	9574	C=0.7257	G=0.0000, T=0.2743
Asian	Sub	736	C=0.753	G=0.000, T=0.247
East Asian	Sub	590	C=0.761	G=0.000, T=0.239
Other Asian	Sub	146	C=0.719	G=0.000, T=0.281
Latin American 1	Sub	784	C=0.584	G=0.000, T=0.416
Latin American 2	Sub	2842	C=0.6840	G=0.0000, T=0.3160
South Asian	Sub	5046	C=0.4851	G=0.0000, T=0.5149
Other	Sub	6818	C=0.5969	G=0.0000, T=0.4031

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	C=0.630213	T=0.369787
Allele Frequency Aggregator	Total	Global	198332	C=0.564352	G=0.000000, T=0.435648
Allele Frequency Aggregator	European	Sub	172192	C=0.553191	G=0.000000, T=0.446809
Allele Frequency Aggregator	African	Sub	9914	C=0.7262	G=0.0000, T=0.2738
Allele Frequency Aggregator	Other	Sub	6818	C=0.5969	G=0.0000, T=0.4031
Allele Frequency Aggregator	South Asian	Sub	5046	C=0.4851	G=0.0000, T=0.5149
Allele Frequency Aggregator	Latin American 2	Sub	2842	C=0.6840	G=0.0000, T=0.3160
Allele Frequency Aggregator	Latin American 1	Sub	784	C=0.584	G=0.000, T=0.416
Allele Frequency Aggregator	Asian	Sub	736	C=0.753	G=0.000, T=0.247
gnomAD - Genomes	Global	Study-wide	135960	C=0.619204	T=0.380796
gnomAD - Genomes	European	Sub	73654	C=0.54251	T=0.45749
gnomAD - Genomes	African	Sub	40478	C=0.72499	T=0.27501
gnomAD - Genomes	American	Sub	13332	C=0.67754	T=0.32246
gnomAD - Genomes	Ashkenazi Jewish	Sub	3304	C=0.6547	T=0.3453
gnomAD - Genomes	East Asian	Sub	3106	C=0.7611	T=0.2389
gnomAD - Genomes	Other	Sub	2086	C=0.6342	T=0.3658
The PAGE Study	Global	Study-wide	78694	C=0.69760	T=0.30240
The PAGE Study	AfricanAmerican	Sub	32508	C=0.71222	T=0.28778
The PAGE Study	Mexican	Sub	10810	C=0.67345	T=0.32655
The PAGE Study	Asian	Sub	8318	C=0.7502	T=0.2498
The PAGE Study	PuertoRican	Sub	7918	C=0.6604	T=0.3396
The PAGE Study	NativeHawaiian	Sub	4534	C=0.7561	T=0.2439
The PAGE Study	Cuban	Sub	4230	C=0.5917	T=0.4083
The PAGE Study	Dominican	Sub	3828	C=0.6708	T=0.3292
The PAGE Study	CentralAmerican	Sub	2450	C=0.7531	T=0.2469
The PAGE Study	SouthAmerican	Sub	1982	C=0.7321	T=0.2679
The PAGE Study	NativeAmerican	Sub	1260	C=0.6103	T=0.3897
The PAGE Study	SouthAsian	Sub	856	C=0.504	T=0.496
14KJPN	JAPANESE	Study-wide	28256	C=0.76762	T=0.23238
8.3KJPN	JAPANESE	Study-wide	16756	C=0.77107	T=0.22893
1000Genomes_30x	Global	Study-wide	6404	C=0.6558	T=0.3442
1000Genomes_30x	African	Sub	1786	C=0.7469	T=0.2531
1000Genomes_30x	Europe	Sub	1266	C=0.5261	T=0.4739
1000Genomes_30x	South Asian	Sub	1202	C=0.4942	T=0.5058
1000Genomes_30x	East Asian	Sub	1170	C=0.7726	T=0.2274
1000Genomes_30x	American	Sub	980	C=0.716	T=0.284
1000Genomes	Global	Study-wide	5008	C=0.6575	T=0.3425
1000Genomes	African	Sub	1322	C=0.7504	T=0.2496
1000Genomes	East Asian	Sub	1008	C=0.7639	T=0.2361
1000Genomes	Europe	Sub	1006	C=0.5408	T=0.4592
1000Genomes	South Asian	Sub	978	C=0.501	T=0.499
1000Genomes	American	Sub	694	C=0.716	T=0.284
Genetic variation in the Estonian population	Estonian	Study-wide	4452	C=0.5721	T=0.4279
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.5317	T=0.4683
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.5343	T=0.4657
KOREAN population from KRGDB	KOREAN	Study-wide	2914	C=0.8082	T=0.1918
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.6795	T=0.3205
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.757	T=0.243
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.495	T=0.505
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.697	T=0.303
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.516	T=0.484
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.831	T=0.169
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.903	T=0.097
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.69	T=0.31
HapMap	Global	Study-wide	1892	C=0.6855	T=0.3145
HapMap	American	Sub	770	C=0.612	T=0.388
HapMap	African	Sub	692	C=0.775	T=0.225
HapMap	Asian	Sub	254	C=0.756	T=0.244
HapMap	Europe	Sub	176	C=0.557	T=0.443
CNV burdens in cranial meningiomas	Global	Study-wide	790	C=0.754	T=0.246
CNV burdens in cranial meningiomas	CRM	Sub	790	C=0.754	T=0.246
Northern Sweden	ACPOP	Study-wide	598	C=0.505	T=0.495
SGDP_PRJ	Global	Study-wide	278	C=0.374	T=0.626
Qatari	Global	Study-wide	216	C=0.745	T=0.255
The Danish reference pan genome	Danish	Study-wide	40	C=0.55	T=0.45
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	40	C=0.45	T=0.55
Siberian	Global	Study-wide	36	C=0.22	T=0.78

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.28391927C>G
GRCh38.p14 chr 2	NC_000002.12:g.28391927C>T
GRCh37.p13 chr 2	NC_000002.11:g.28614794C>G
GRCh37.p13 chr 2	NC_000002.11:g.28614794C>T

Gene: FOSL2, FOS like 2, AP-1 transcription factor subunit (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
FOSL2 transcript	NM_005253.4:c.	N/A	Upstream Transcript Variant
FOSL2 transcript variant X3	XM_005264231.5:c.	N/A	Upstream Transcript Variant
FOSL2 transcript variant X1	XM_006711976.4:c.	N/A	Upstream Transcript Variant
FOSL2 transcript variant X2	XM_006711977.4:c.	N/A	N/A

Gene: FOSL2-AS1, FOSL2 antisense RNA 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FOSL2-AS1 transcript	NR_103831.1:n.	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	C=	G	T
GRCh38.p14 chr 2	NC_000002.12:g.28391927=	NC_000002.12:g.28391927C>G	NC_000002.12:g.28391927C>T
GRCh37.p13 chr 2	NC_000002.11:g.28614794=	NC_000002.11:g.28614794C>G	NC_000002.11:g.28614794C>T

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#.

125 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss1362702	Oct 05, 2000 (86)
2	SC_SNP	ss15438304	Feb 27, 2004 (120)
3	ILLUMINA	ss66727023	Nov 29, 2006 (127)
4	ILLUMINA	ss67896458	Nov 29, 2006 (127)
5	ILLUMINA	ss68030630	Nov 29, 2006 (127)
6	PERLEGEN	ss68807628	May 16, 2007 (127)
7	ILLUMINA	ss71595280	May 16, 2007 (127)
8	ILLUMINA	ss75634273	Dec 07, 2007 (129)
9	ILLUMINA	ss79290013	Dec 15, 2007 (130)
10	KRIBB_YJKIM	ss83614805	Dec 15, 2007 (130)
11	BCMHGSC_JDW	ss91098139	Mar 24, 2008 (129)
12	ILLUMINA	ss98237914	May 26, 2008 (130)
13	1000GENOMES	ss109351511	Jan 24, 2009 (130)
14	1000GENOMES	ss109993111	Jan 24, 2009 (130)
15	ILLUMINA-UK	ss117634592	Feb 14, 2009 (130)
16	ILLUMINA	ss122953846	Dec 01, 2009 (131)
17	ILLUMINA	ss154482253	Dec 01, 2009 (131)
18	GMI	ss156837658	Dec 01, 2009 (131)
19	ILLUMINA	ss159656665	Dec 01, 2009 (131)
20	ILLUMINA	ss160968849	Dec 01, 2009 (131)
21	COMPLETE_GENOMICS	ss163225254	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss164057568	Jul 04, 2010 (132)
23	ILLUMINA	ss172434566	Jul 04, 2010 (132)
24	ILLUMINA	ss174787553	Jul 04, 2010 (132)
25	BCM-HGSC-SUB	ss205945648	Jul 04, 2010 (132)
26	ILLUMINA	ss209093520	Jul 04, 2010 (132)
27	1000GENOMES	ss219136572	Jul 14, 2010 (132)
28	1000GENOMES	ss231088121	Jul 14, 2010 (132)
29	1000GENOMES	ss238661181	Jul 15, 2010 (132)
30	BL	ss252991984	May 09, 2011 (134)
31	GMI	ss276396414	May 04, 2012 (137)
32	GMI	ss284313448	Apr 25, 2013 (138)
33	ILLUMINA	ss481846034	May 04, 2012 (137)
34	ILLUMINA	ss481878670	May 04, 2012 (137)
35	ILLUMINA	ss482835278	Sep 08, 2015 (146)
36	ILLUMINA	ss485717442	May 04, 2012 (137)
37	ILLUMINA	ss537577910	Sep 08, 2015 (146)
38	TISHKOFF	ss555435967	Apr 25, 2013 (138)
39	SSMP	ss649016517	Apr 25, 2013 (138)
40	ILLUMINA	ss779004364	Aug 21, 2014 (142)
41	ILLUMINA	ss783304372	Aug 21, 2014 (142)
42	ILLUMINA	ss784256558	Aug 21, 2014 (142)
43	ILLUMINA	ss825620531	Jul 19, 2016 (147)
44	ILLUMINA	ss832565749	Apr 01, 2015 (144)
45	ILLUMINA	ss833167458	Aug 21, 2014 (142)
46	ILLUMINA	ss833758286	Aug 21, 2014 (142)
47	ILLUMINA	ss834466768	Aug 21, 2014 (142)
48	EVA-GONL	ss976620406	Aug 21, 2014 (142)
49	JMKIDD_LAB	ss1068956407	Aug 21, 2014 (142)
50	1000GENOMES	ss1296419980	Aug 21, 2014 (142)
51	DDI	ss1428516015	Apr 01, 2015 (144)
52	EVA_GENOME_DK	ss1578792601	Apr 01, 2015 (144)
53	EVA_DECODE	ss1586025731	Apr 01, 2015 (144)
54	EVA_UK10K_ALSPAC	ss1603080900	Apr 01, 2015 (144)
55	EVA_UK10K_TWINSUK	ss1646074933	Apr 01, 2015 (144)
56	EVA_SVP	ss1712440529	Apr 01, 2015 (144)
57	ILLUMINA	ss1752350963	Sep 08, 2015 (146)
58	WEILL_CORNELL_DGM	ss1919852827	Feb 12, 2016 (147)
59	ILLUMINA	ss1958400775	Feb 12, 2016 (147)
60	GENOMED	ss1968722923	Jul 19, 2016 (147)
61	ILLUMINA	ss2094805783	Dec 20, 2016 (150)
62	ILLUMINA	ss2095088894	Dec 20, 2016 (150)
63	USC_VALOUEV	ss2148499165	Dec 20, 2016 (150)
64	SYSTEMSBIOZJU	ss2624742625	Nov 08, 2017 (151)
65	ILLUMINA	ss2633588190	Nov 08, 2017 (151)
66	GRF	ss2703060189	Nov 08, 2017 (151)
67	GNOMAD	ss2771170904	Nov 08, 2017 (151)
68	AFFY	ss2985162809	Nov 08, 2017 (151)
69	AFFY	ss2985786961	Nov 08, 2017 (151)
70	SWEGEN	ss2989182510	Nov 08, 2017 (151)
71	ILLUMINA	ss3021953175	Nov 08, 2017 (151)
72	BIOINF_KMB_FNS_UNIBA	ss3023993533	Nov 08, 2017 (151)
73	CSHL	ss3344132740	Nov 08, 2017 (151)
74	ILLUMINA	ss3628020090	Oct 11, 2018 (152)
75	ILLUMINA	ss3631556665	Oct 11, 2018 (152)
76	ILLUMINA	ss3633193113	Oct 11, 2018 (152)
77	ILLUMINA	ss3633904458	Oct 11, 2018 (152)
78	ILLUMINA	ss3634757197	Oct 11, 2018 (152)
79	ILLUMINA	ss3635590901	Oct 11, 2018 (152)
80	ILLUMINA	ss3636442997	Oct 11, 2018 (152)
81	ILLUMINA	ss3637342729	Oct 11, 2018 (152)
82	ILLUMINA	ss3638249246	Oct 11, 2018 (152)
83	ILLUMINA	ss3639129280	Oct 11, 2018 (152)
84	ILLUMINA	ss3639576101	Oct 11, 2018 (152)
85	ILLUMINA	ss3640464500	Oct 11, 2018 (152)
86	ILLUMINA	ss3643220199	Oct 11, 2018 (152)
87	ILLUMINA	ss3652382564	Oct 11, 2018 (152)
88	EGCUT_WGS	ss3657136942	Jul 13, 2019 (153)
89	EVA_DECODE	ss3703500992	Jul 13, 2019 (153)
90	ILLUMINA	ss3725768609	Jul 13, 2019 (153)
91	ACPOP	ss3728261693	Jul 13, 2019 (153)
92	ILLUMINA	ss3745057146	Jul 13, 2019 (153)
93	EVA	ss3756510857	Jul 13, 2019 (153)
94	PAGE_CC	ss3770905591	Jul 13, 2019 (153)
95	ILLUMINA	ss3772554021	Jul 13, 2019 (153)
96	KHV_HUMAN_GENOMES	ss3800890515	Jul 13, 2019 (153)
97	EVA	ss3826883296	Apr 25, 2020 (154)
98	EVA	ss3836848771	Apr 25, 2020 (154)
99	EVA	ss3842263392	Apr 25, 2020 (154)
100	HGDP	ss3847610744	Apr 25, 2020 (154)
101	SGDP_PRJ	ss3851855126	Apr 25, 2020 (154)
102	KRGDB	ss3897271494	Apr 25, 2020 (154)
103	EVA	ss3984479444	Apr 26, 2021 (155)
104	EVA	ss3984880975	Apr 26, 2021 (155)
105	EVA	ss4016986090	Apr 26, 2021 (155)
106	TOPMED	ss4498593403	Apr 26, 2021 (155)
107	TOMMO_GENOMICS	ss5150447529	Apr 26, 2021 (155)
108	1000G_HIGH_COVERAGE	ss5247359188	Oct 17, 2022 (156)
109	EVA	ss5314719550	Oct 17, 2022 (156)
110	EVA	ss5327632511	Oct 17, 2022 (156)
111	HUGCELL_USP	ss5447626888	Oct 17, 2022 (156)
112	EVA	ss5506335071	Oct 17, 2022 (156)
113	1000G_HIGH_COVERAGE	ss5522209372	Oct 17, 2022 (156)
114	SANFORD_IMAGENETICS	ss5624439903	Oct 17, 2022 (156)
115	SANFORD_IMAGENETICS	ss5628343810	Oct 17, 2022 (156)
116	TOMMO_GENOMICS	ss5678807978	Oct 17, 2022 (156)
117	EVA	ss5799525781	Oct 17, 2022 (156)
118	YY_MCH	ss5802033335	Oct 17, 2022 (156)
119	EVA	ss5819827079	Oct 17, 2022 (156)
120	EVA	ss5847184141	Oct 17, 2022 (156)
121	EVA	ss5847860932	Oct 17, 2022 (156)
122	EVA	ss5852441590	Oct 17, 2022 (156)
123	EVA	ss5929543483	Oct 17, 2022 (156)
124	EVA	ss5954546979	Oct 17, 2022 (156)
125	EVA	ss5979560482	Oct 17, 2022 (156)
126	1000Genomes	NC_000002.11 - 28614794	Oct 11, 2018 (152)
127	1000Genomes_30x	NC_000002.12 - 28391927	Oct 17, 2022 (156)
128	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 28614794	Oct 11, 2018 (152)
129	Genetic variation in the Estonian population	NC_000002.11 - 28614794	Oct 11, 2018 (152)
130	The Danish reference pan genome	NC_000002.11 - 28614794	Apr 25, 2020 (154)
131	gnomAD - Genomes	NC_000002.12 - 28391927	Apr 26, 2021 (155)
132	HGDP-CEPH-db Supplement 1	NC_000002.10 - 28468298	Apr 25, 2020 (154)
133	HapMap	NC_000002.12 - 28391927	Apr 25, 2020 (154)
134	KOREAN population from KRGDB	NC_000002.11 - 28614794	Apr 25, 2020 (154)
135	Northern Sweden	NC_000002.11 - 28614794	Jul 13, 2019 (153)
136	The PAGE Study	NC_000002.12 - 28391927	Jul 13, 2019 (153)
137	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000002.11 - 28614794	Apr 26, 2021 (155)
138	CNV burdens in cranial meningiomas	NC_000002.11 - 28614794	Apr 26, 2021 (155)
139	Qatari	NC_000002.11 - 28614794	Apr 25, 2020 (154)
140	SGDP_PRJ	NC_000002.11 - 28614794	Apr 25, 2020 (154)
141	Siberian	NC_000002.11 - 28614794	Apr 25, 2020 (154)
142	8.3KJPN	NC_000002.11 - 28614794	Apr 26, 2021 (155)
143	14KJPN	NC_000002.12 - 28391927	Oct 17, 2022 (156)
144	TopMed	NC_000002.12 - 28391927	Apr 26, 2021 (155)
145	UK 10K study - Twins	NC_000002.11 - 28614794	Oct 11, 2018 (152)
146	ALFA	NC_000002.12 - 28391927	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)
rs60802663	May 26, 2008 (130)
rs386621155	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
5609470582	NC_000002.12:28391926:C:G	NC_000002.12:28391926:C:G	(self)
ss3639129280, ss3639576101	NC_000002.9:28526444:C:T	NC_000002.12:28391926:C:T	(self)
288636, ss91098139, ss109351511, ss109993111, ss117634592, ss163225254, ss164057568, ss205945648, ss252991984, ss276396414, ss284313448, ss481846034, ss825620531, ss1586025731, ss1712440529, ss3643220199, ss3847610744	NC_000002.10:28468297:C:T	NC_000002.12:28391926:C:T	(self)
7339180, 4074134, 2875190, 4968569, 4448888, 1546558, 106902, 28770, 1894757, 3872106, 1015519, 8416836, 4074134, ss219136572, ss231088121, ss238661181, ss481878670, ss482835278, ss485717442, ss537577910, ss555435967, ss649016517, ss779004364, ss783304372, ss784256558, ss832565749, ss833167458, ss833758286, ss834466768, ss976620406, ss1068956407, ss1296419980, ss1428516015, ss1578792601, ss1603080900, ss1646074933, ss1752350963, ss1919852827, ss1958400775, ss1968722923, ss2094805783, ss2095088894, ss2148499165, ss2624742625, ss2633588190, ss2703060189, ss2771170904, ss2985162809, ss2985786961, ss2989182510, ss3021953175, ss3344132740, ss3628020090, ss3631556665, ss3633193113, ss3633904458, ss3634757197, ss3635590901, ss3636442997, ss3637342729, ss3638249246, ss3640464500, ss3652382564, ss3657136942, ss3728261693, ss3745057146, ss3756510857, ss3772554021, ss3826883296, ss3836848771, ss3851855126, ss3897271494, ss3984479444, ss3984880975, ss4016986090, ss5150447529, ss5314719550, ss5327632511, ss5506335071, ss5624439903, ss5628343810, ss5799525781, ss5819827079, ss5847184141, ss5847860932, ss5954546979, ss5979560482	NC_000002.11:28614793:C:T	NC_000002.12:28391926:C:T	(self)
9735307, 52160016, 1759496, 127060, 12645082, 302416282, 5609470582, ss3023993533, ss3703500992, ss3725768609, ss3770905591, ss3800890515, ss3842263392, ss4498593403, ss5247359188, ss5447626888, ss5522209372, ss5678807978, ss5802033335, ss5852441590, ss5929543483	NC_000002.12:28391926:C:T	NC_000002.12:28391926:C:T	(self)
ss15438304	NT_022184.13:7430726:C:T	NC_000002.12:28391926:C:T	(self)
ss1362702, ss66727023, ss67896458, ss68030630, ss68807628, ss71595280, ss75634273, ss79290013, ss83614805, ss98237914, ss122953846, ss154482253, ss156837658, ss159656665, ss160968849, ss172434566, ss174787553, ss209093520	NT_022184.15:7436680:C:T	NC_000002.12:28391926:C:T	(self)

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

5 citations for rs925255

PMID	Title	Author	Year	Journal
24587880	Association Study of FOS-Like Antigen-2 Promoter Polymorphisms With Papillary Thyroid Cancer in Korean Population.	Kim SW et al.	2014	Clinical and experimental otorhinolaryngology
24652774	Association of FOS-like antigen 1 promoter polymorphism with podocyte foot process effacement in immunoglobulin A nephropathy patients.	Park HJ et al.	2014	Journal of clinical laboratory analysis
27156530	Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility.	Ye BD et al.	2016	Expert review of clinical immunology
27336838	Blood and Intestine eQTLs from an Anti-TNF-Resistant Crohn's Disease Cohort Inform IBD Genetic Association Loci.	Di Narzo AF et al.	2016	Clinical and translational gastroenterology
27903283	Systematic analysis of chromatin interactions at disease associated loci links novel candidate genes to inflammatory bowel disease.	Meddens CA et al.	2016	Genome biology

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

rs925255