Name: rs145209802
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.

rs145209802

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:48415288-48415290 (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: delG / dupG
Variation Type: Indel Insertion and Deletion
Frequency: delG=0.181907 (48149/264690, TOPMED)
delG=0.197534 (27648/139966, GnomAD)
delG=0.25756 (7278/28258, 14KJPN) (+ 12 more)
delG=0.22981 (4256/18520, ALFA)
delG=0.25200 (4223/16758, 8.3KJPN)
delG=0.1641 (1051/6404, 1000G_30x)
delG=0.1673 (838/5008, 1000G)
delG=0.3719 (1666/4480, Estonian)
delG=0.2097 (808/3854, ALSPAC)
delG=0.2001 (742/3708, TWINSUK)
delG=0.3002 (550/1832, Korea1K)
delG=0.245 (245/998, GoNL)
delG=0.243 (146/600, NorthernSweden)
delG=0.167 (35/210, Vietnamese)
delG=0.12 (5/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ABCA13 : 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	18520	GGG=0.77019	GG=0.22981
European	Sub	14152	GGG=0.74915	GG=0.25085
African	Sub	2898	GGG=0.8537	GG=0.1463
African Others	Sub	114	GGG=0.877	GG=0.123
African American	Sub	2784	GGG=0.8527	GG=0.1473
Asian	Sub	112	GGG=0.830	GG=0.170
East Asian	Sub	86	GGG=0.83	GG=0.17
Other Asian	Sub	26	GGG=0.85	GG=0.15
Latin American 1	Sub	146	GGG=0.904	GG=0.096
Latin American 2	Sub	610	GGG=0.780	GG=0.220
South Asian	Sub	98	GGG=0.85	GG=0.15
Other	Sub	504	GGG=0.802	GG=0.198

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	GGG=0.818093	delG=0.181907
gnomAD - Genomes	Global	Study-wide	139966	GGG=0.802466	delG=0.197534
gnomAD - Genomes	European	Sub	75780	GGG=0.77249	delG=0.22751
gnomAD - Genomes	African	Sub	41964	GGG=0.86391	delG=0.13609
gnomAD - Genomes	American	Sub	13626	GGG=0.77954	delG=0.22046
gnomAD - Genomes	Ashkenazi Jewish	Sub	3312	GGG=0.8478	delG=0.1522
gnomAD - Genomes	East Asian	Sub	3132	GGG=0.7497	delG=0.2503
gnomAD - Genomes	Other	Sub	2152	GGG=0.8123	delG=0.1877
14KJPN	JAPANESE	Study-wide	28258	GGG=0.74244	delG=0.25756
Allele Frequency Aggregator	Total	Global	18520	GGG=0.77019	delG=0.22981
Allele Frequency Aggregator	European	Sub	14152	GGG=0.74915	delG=0.25085
Allele Frequency Aggregator	African	Sub	2898	GGG=0.8537	delG=0.1463
Allele Frequency Aggregator	Latin American 2	Sub	610	GGG=0.780	delG=0.220
Allele Frequency Aggregator	Other	Sub	504	GGG=0.802	delG=0.198
Allele Frequency Aggregator	Latin American 1	Sub	146	GGG=0.904	delG=0.096
Allele Frequency Aggregator	Asian	Sub	112	GGG=0.830	delG=0.170
Allele Frequency Aggregator	South Asian	Sub	98	GGG=0.85	delG=0.15
8.3KJPN	JAPANESE	Study-wide	16758	GGG=0.74800	delG=0.25200
1000Genomes_30x	Global	Study-wide	6404	GGG=0.8359	delG=0.1641
1000Genomes_30x	African	Sub	1786	GGG=0.8606	delG=0.1394
1000Genomes_30x	Europe	Sub	1266	GGG=0.8025	delG=0.1975
1000Genomes_30x	South Asian	Sub	1202	GGG=0.9077	delG=0.0923
1000Genomes_30x	East Asian	Sub	1170	GGG=0.7846	delG=0.2154
1000Genomes_30x	American	Sub	980	GGG=0.807	delG=0.193
1000Genomes	Global	Study-wide	5008	GGG=0.8327	delG=0.1673
1000Genomes	African	Sub	1322	GGG=0.8578	delG=0.1422
1000Genomes	East Asian	Sub	1008	GGG=0.7817	delG=0.2183
1000Genomes	Europe	Sub	1006	GGG=0.7982	delG=0.2018
1000Genomes	South Asian	Sub	978	GGG=0.907	delG=0.093
1000Genomes	American	Sub	694	GGG=0.804	delG=0.196
Genetic variation in the Estonian population	Estonian	Study-wide	4480	GGG=0.6281	delG=0.3719
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	GGG=0.7903	delG=0.2097
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	GGG=0.7999	delG=0.2001
Korean Genome Project	KOREAN	Study-wide	1832	GGG=0.6998	delG=0.3002
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	GGG=0.755	delG=0.245
Northern Sweden	ACPOP	Study-wide	600	GGG=0.757	delG=0.243
A Vietnamese Genetic Variation Database	Global	Study-wide	210	GGG=0.833	delG=0.167
The Danish reference pan genome	Danish	Study-wide	40	GGG=0.88	delG=0.12

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 7	NC_000007.14:g.48415290del
GRCh38.p14 chr 7	NC_000007.14:g.48415290dup
GRCh37.p13 chr 7	NC_000007.13:g.48454887del
GRCh37.p13 chr 7	NC_000007.13:g.48454887dup
ABCA13 RefSeqGene	NG_012385.2:g.248831del
ABCA13 RefSeqGene	NG_012385.2:g.248831dup

Gene: ABCA13, ATP binding cassette subfamily A member 13 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ABCA13 transcript	NM_152701.5:c.12459+2707d… NM_152701.5:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X1	XM_011515130.3:c.12459+27… XM_011515130.3:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X2	XM_011515131.3:c.12459+27… XM_011515131.3:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X3	XM_011515132.3:c.12459+27… XM_011515132.3:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X4	XM_011515133.3:c.12321+27… XM_011515133.3:c.12321+2707del	N/A	Intron Variant
ABCA13 transcript variant X8	XM_011515134.3:c.12459+27… XM_011515134.3:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X9	XM_011515136.2:c.11865+27… XM_011515136.2:c.11865+2707del	N/A	Intron Variant
ABCA13 transcript variant X13	XM_011515137.4:c.12459+27… XM_011515137.4:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X16	XM_011515138.3:c.12459+27… XM_011515138.3:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X17	XM_011515139.3:c.12459+27… XM_011515139.3:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X20	XM_011515141.3:c.12459+27… XM_011515141.3:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X21	XM_011515142.3:c.12459+27… XM_011515142.3:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X18	XM_017011767.2:c.12459+27… XM_017011767.2:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X19	XM_017011768.2:c.12459+27… XM_017011768.2:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X5	XM_047419918.1:c.12459+27… XM_047419918.1:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X10	XM_047419919.1:c.12459+27… XM_047419919.1:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X11	XM_047419920.1:c.12459+27… XM_047419920.1:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X12	XM_047419921.1:c.12459+27… XM_047419921.1:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X14	XM_047419922.1:c.12459+27… XM_047419922.1:c.12459+2707del	N/A	Intron Variant
ABCA13 transcript variant X22	XM_011515143.3:c.	N/A	Genic Downstream Transcript Variant
ABCA13 transcript variant X23	XM_011515144.3:c.	N/A	Genic Downstream Transcript Variant
ABCA13 transcript variant X24	XM_011515145.3:c.	N/A	Genic Downstream Transcript Variant
ABCA13 transcript variant X25	XM_011515146.3:c.	N/A	Genic Downstream Transcript Variant
ABCA13 transcript variant X26	XM_011515147.3:c.	N/A	Genic Downstream Transcript Variant
ABCA13 transcript variant X27	XM_011515148.3:c.	N/A	Genic Downstream Transcript Variant
ABCA13 transcript variant X28	XM_011515149.3:c.	N/A	Genic Downstream Transcript Variant
ABCA13 transcript variant X6	XR_926914.3:n.	N/A	Intron Variant
ABCA13 transcript variant X7	XR_926915.3:n.	N/A	Intron Variant
ABCA13 transcript variant X15	XR_926919.3: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	GGG=	delG	dupG
GRCh38.p14 chr 7	NC_000007.14:g.48415288_48415290=	NC_000007.14:g.48415290del	NC_000007.14:g.48415290dup
GRCh37.p13 chr 7	NC_000007.13:g.48454885_48454887=	NC_000007.13:g.48454887del	NC_000007.13:g.48454887dup
ABCA13 RefSeqGene	NG_012385.2:g.248829_248831=	NG_012385.2:g.248831del	NG_012385.2:g.248831dup
ABCA13 transcript	NM_152701.3:c.12459+2705=	NM_152701.3:c.12459+2707del	NM_152701.3:c.12459+2707dup
ABCA13 transcript	NM_152701.5:c.12459+2705=	NM_152701.5:c.12459+2707del	NM_152701.5:c.12459+2707dup
ABCA13 transcript variant X1	XM_005249623.1:c.5502+2705=	XM_005249623.1:c.5502+2707del	XM_005249623.1:c.5502+2707dup
ABCA13 transcript variant X2	XM_005249624.1:c.5502+2705=	XM_005249624.1:c.5502+2707del	XM_005249624.1:c.5502+2707dup
ABCA13 transcript variant X3	XM_005249625.1:c.5502+2705=	XM_005249625.1:c.5502+2707del	XM_005249625.1:c.5502+2707dup
ABCA13 transcript variant X1	XM_011515130.3:c.12459+2705=	XM_011515130.3:c.12459+2707del	XM_011515130.3:c.12459+2707dup
ABCA13 transcript variant X2	XM_011515131.3:c.12459+2705=	XM_011515131.3:c.12459+2707del	XM_011515131.3:c.12459+2707dup
ABCA13 transcript variant X3	XM_011515132.3:c.12459+2705=	XM_011515132.3:c.12459+2707del	XM_011515132.3:c.12459+2707dup
ABCA13 transcript variant X4	XM_011515133.3:c.12321+2705=	XM_011515133.3:c.12321+2707del	XM_011515133.3:c.12321+2707dup
ABCA13 transcript variant X8	XM_011515134.3:c.12459+2705=	XM_011515134.3:c.12459+2707del	XM_011515134.3:c.12459+2707dup
ABCA13 transcript variant X9	XM_011515136.2:c.11865+2705=	XM_011515136.2:c.11865+2707del	XM_011515136.2:c.11865+2707dup
ABCA13 transcript variant X13	XM_011515137.4:c.12459+2705=	XM_011515137.4:c.12459+2707del	XM_011515137.4:c.12459+2707dup
ABCA13 transcript variant X16	XM_011515138.3:c.12459+2705=	XM_011515138.3:c.12459+2707del	XM_011515138.3:c.12459+2707dup
ABCA13 transcript variant X17	XM_011515139.3:c.12459+2705=	XM_011515139.3:c.12459+2707del	XM_011515139.3:c.12459+2707dup
ABCA13 transcript variant X20	XM_011515141.3:c.12459+2705=	XM_011515141.3:c.12459+2707del	XM_011515141.3:c.12459+2707dup
ABCA13 transcript variant X21	XM_011515142.3:c.12459+2705=	XM_011515142.3:c.12459+2707del	XM_011515142.3:c.12459+2707dup
ABCA13 transcript variant X18	XM_017011767.2:c.12459+2705=	XM_017011767.2:c.12459+2707del	XM_017011767.2:c.12459+2707dup
ABCA13 transcript variant X19	XM_017011768.2:c.12459+2705=	XM_017011768.2:c.12459+2707del	XM_017011768.2:c.12459+2707dup
ABCA13 transcript variant X5	XM_047419918.1:c.12459+2705=	XM_047419918.1:c.12459+2707del	XM_047419918.1:c.12459+2707dup
ABCA13 transcript variant X10	XM_047419919.1:c.12459+2705=	XM_047419919.1:c.12459+2707del	XM_047419919.1:c.12459+2707dup
ABCA13 transcript variant X11	XM_047419920.1:c.12459+2705=	XM_047419920.1:c.12459+2707del	XM_047419920.1:c.12459+2707dup
ABCA13 transcript variant X12	XM_047419921.1:c.12459+2705=	XM_047419921.1:c.12459+2707del	XM_047419921.1:c.12459+2707dup
ABCA13 transcript variant X14	XM_047419922.1:c.12459+2705=	XM_047419922.1:c.12459+2707del	XM_047419922.1:c.12459+2707dup

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#.

48 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GMI	ss287812325	May 09, 2011 (137)
2	GMI	ss288839226	May 04, 2012 (137)
3	1000GENOMES	ss326932335	May 09, 2011 (134)
4	1000GENOMES	ss326985842	May 09, 2011 (134)
5	1000GENOMES	ss327271135	May 09, 2011 (134)
6	1000GENOMES	ss499856465	May 04, 2012 (137)
7	LUNTER	ss551730929	Apr 25, 2013 (138)
8	LUNTER	ss551937126	Apr 25, 2013 (138)
9	LUNTER	ss553296011	Apr 25, 2013 (138)
10	TISHKOFF	ss554334163	Apr 25, 2013 (138)
11	SSMP	ss663782396	Apr 01, 2015 (144)
12	BILGI_BIOE	ss666396712	Apr 25, 2013 (138)
13	EVA-GONL	ss984244097	Aug 21, 2014 (142)
14	1000GENOMES	ss1377063760	Aug 21, 2014 (142)
15	EVA_GENOME_DK	ss1576985684	Apr 01, 2015 (144)
16	EVA_DECODE	ss1593820950	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1705621711	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1705621757	Apr 01, 2015 (144)
19	JJLAB	ss2030838396	Sep 14, 2016 (149)
20	SYSTEMSBIOZJU	ss2626700654	Nov 08, 2017 (151)
21	GNOMAD	ss2852807482	Nov 08, 2017 (151)
22	SWEGEN	ss3001068277	Nov 08, 2017 (151)
23	BEROUKHIMLAB	ss3644237234	Oct 12, 2018 (152)
24	BIOINF_KMB_FNS_UNIBA	ss3646026315	Oct 12, 2018 (152)
25	EGCUT_WGS	ss3668990159	Jul 13, 2019 (153)
26	EVA_DECODE	ss3719635276	Jul 13, 2019 (153)
27	ACPOP	ss3734603697	Jul 13, 2019 (153)
28	PACBIO	ss3785808747	Jul 13, 2019 (153)
29	PACBIO	ss3791111739	Jul 13, 2019 (153)
30	PACBIO	ss3795991695	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3809686382	Jul 13, 2019 (153)
32	EVA	ss3830557000	Apr 26, 2020 (154)
33	EVA	ss3838766682	Apr 26, 2020 (154)
34	EVA	ss3844218804	Apr 26, 2020 (154)
35	KOGIC	ss3961410060	Apr 26, 2020 (154)
36	TOPMED	ss4744952328	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5183019806	Apr 26, 2021 (155)
38	1000G_HIGH_COVERAGE	ss5272772632	Oct 14, 2022 (156)
39	HUGCELL_USP	ss5469956888	Oct 14, 2022 (156)
40	EVA	ss5508944400	Oct 14, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5560886973	Oct 14, 2022 (156)
42	SANFORD_IMAGENETICS	ss5642888531	Oct 14, 2022 (156)
43	TOMMO_GENOMICS	ss5722818269	Oct 14, 2022 (156)
44	YY_MCH	ss5808574082	Oct 14, 2022 (156)
45	EVA	ss5822780791	Oct 14, 2022 (156)
46	EVA	ss5855880465	Oct 14, 2022 (156)
47	EVA	ss5858788924	Oct 14, 2022 (156)
48	EVA	ss5972104195	Oct 14, 2022 (156)
49	1000Genomes	NC_000007.13 - 48454885	Oct 12, 2018 (152)
50	1000Genomes_30x	NC_000007.14 - 48415288	Oct 14, 2022 (156)
51	The Avon Longitudinal Study of Parents and Children	NC_000007.13 - 48454885	Oct 12, 2018 (152)
52	Genetic variation in the Estonian population	NC_000007.13 - 48454885	Oct 12, 2018 (152)
53	The Danish reference pan genome	NC_000007.13 - 48454885	Apr 26, 2020 (154)
54	gnomAD - Genomes	NC_000007.14 - 48415288	Apr 26, 2021 (155)
55	Genome of the Netherlands Release 5	NC_000007.13 - 48454885	Apr 26, 2020 (154)
56	Korean Genome Project	NC_000007.14 - 48415288	Apr 26, 2020 (154)
57	Northern Sweden	NC_000007.13 - 48454885	Jul 13, 2019 (153)
58	8.3KJPN	NC_000007.13 - 48454885	Apr 26, 2021 (155)
59	14KJPN	NC_000007.14 - 48415288	Oct 14, 2022 (156)
60	TopMed	NC_000007.14 - 48415288	Apr 26, 2021 (155)
61	UK 10K study - Twins	NC_000007.13 - 48454885	Oct 12, 2018 (152)
62	A Vietnamese Genetic Variation Database	NC_000007.13 - 48454885	Jul 13, 2019 (153)
63	ALFA	NC_000007.14 - 48415288	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)
rs145917394	May 04, 2012 (137)
rs373905446	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss288839226, ss326932335, ss326985842, ss327271135, ss551730929, ss551937126, ss553296011, ss1593820950	NC_000007.12:48425430:G:	NC_000007.14:48415287:GGG:GG	(self)
36975056, 20621073, 14728407, 1149181, 9195230, 7888562, 40989113, 20621073, 4595307, ss499856465, ss663782396, ss666396712, ss984244097, ss1377063760, ss1576985684, ss1705621711, ss1705621757, ss2030838396, ss2626700654, ss2852807482, ss3001068277, ss3644237234, ss3668990159, ss3734603697, ss3785808747, ss3791111739, ss3795991695, ss3830557000, ss3838766682, ss5183019806, ss5642888531, ss5822780791, ss5972104195	NC_000007.13:48454884:G:	NC_000007.14:48415287:GGG:GG	(self)
ss554334163	NC_000007.13:48454886:G:	NC_000007.14:48415287:GGG:GG	(self)
48412908, 260636219, 17788061, 56655373, 582329887, ss3646026315, ss3719635276, ss3809686382, ss3844218804, ss3961410060, ss4744952328, ss5272772632, ss5469956888, ss5560886973, ss5722818269, ss5808574082, ss5855880465, ss5858788924	NC_000007.14:48415287:G:	NC_000007.14:48415287:GGG:GG	(self)
11408790652	NC_000007.14:48415287:GGG:GG	NC_000007.14:48415287:GGG:GG	(self)
ss287812325	NT_007819.17:48444884:G:	NC_000007.14:48415287:GGG:GG	(self)
ss5508944400	NC_000007.13:48454884::G	NC_000007.14:48415287:GGG:GGGG

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

No publications for rs145209802

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs145209802