Name: rs9322330
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.

rs9322330

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:151752183 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.081027 (21447/264690, TOPMED)
A=0.068682 (9626/140154, GnomAD)
A=0.04645 (1670/35952, ALFA) (+ 19 more)
A=0.30989 (8757/28258, 14KJPN)
A=0.30973 (5191/16760, 8.3KJPN)
A=0.1270 (813/6404, 1000G_30x)
A=0.1312 (657/5008, 1000G)
A=0.0426 (191/4480, Estonian)
A=0.0125 (48/3854, ALSPAC)
A=0.0092 (34/3708, TWINSUK)
A=0.2706 (793/2930, KOREAN)
A=0.1312 (248/1890, HapMap)
A=0.2898 (531/1832, Korea1K)
A=0.0512 (58/1132, Daghestan)
A=0.006 (6/998, GoNL)
A=0.222 (139/626, Chileans)
A=0.045 (27/600, NorthernSweden)
A=0.028 (6/216, Qatari)
A=0.184 (39/212, Vietnamese)
G=0.401 (61/152, SGDP_PRJ)
A=0.03 (1/40, GENOME_DK)
G=0.30 (6/20, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ESR1 : Intron Variant
LOC107986529 : Non Coding Transcript 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	35952	G=0.95355	A=0.04645
European	Sub	26124	G=0.98090	A=0.01910
African	Sub	3846	G=0.8869	A=0.1131
African Others	Sub	136	G=0.882	A=0.118
African American	Sub	3710	G=0.8871	A=0.1129
Asian	Sub	176	G=0.648	A=0.352
East Asian	Sub	116	G=0.672	A=0.328
Other Asian	Sub	60	G=0.60	A=0.40
Latin American 1	Sub	314	G=0.927	A=0.073
Latin American 2	Sub	2860	G=0.8500	A=0.1500
South Asian	Sub	126	G=0.929	A=0.071
Other	Sub	2506	G=0.9150	A=0.0850

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=0.918973	A=0.081027
gnomAD - Genomes	Global	Study-wide	140154	G=0.931318	A=0.068682
gnomAD - Genomes	European	Sub	75926	G=0.97893	A=0.02107
gnomAD - Genomes	African	Sub	41982	G=0.88245	A=0.11755
gnomAD - Genomes	American	Sub	13642	G=0.85471	A=0.14529
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	G=0.9825	A=0.0175
gnomAD - Genomes	East Asian	Sub	3128	G=0.7203	A=0.2797
gnomAD - Genomes	Other	Sub	2154	G=0.9183	A=0.0817
Allele Frequency Aggregator	Total	Global	35952	G=0.95355	A=0.04645
Allele Frequency Aggregator	European	Sub	26124	G=0.98090	A=0.01910
Allele Frequency Aggregator	African	Sub	3846	G=0.8869	A=0.1131
Allele Frequency Aggregator	Latin American 2	Sub	2860	G=0.8500	A=0.1500
Allele Frequency Aggregator	Other	Sub	2506	G=0.9150	A=0.0850
Allele Frequency Aggregator	Latin American 1	Sub	314	G=0.927	A=0.073
Allele Frequency Aggregator	Asian	Sub	176	G=0.648	A=0.352
Allele Frequency Aggregator	South Asian	Sub	126	G=0.929	A=0.071
14KJPN	JAPANESE	Study-wide	28258	G=0.69011	A=0.30989
8.3KJPN	JAPANESE	Study-wide	16760	G=0.69027	A=0.30973
1000Genomes_30x	Global	Study-wide	6404	G=0.8730	A=0.1270
1000Genomes_30x	African	Sub	1786	G=0.8830	A=0.1170
1000Genomes_30x	Europe	Sub	1266	G=0.9858	A=0.0142
1000Genomes_30x	South Asian	Sub	1202	G=0.8819	A=0.1181
1000Genomes_30x	East Asian	Sub	1170	G=0.7530	A=0.2470
1000Genomes_30x	American	Sub	980	G=0.842	A=0.158
1000Genomes	Global	Study-wide	5008	G=0.8688	A=0.1312
1000Genomes	African	Sub	1322	G=0.8828	A=0.1172
1000Genomes	East Asian	Sub	1008	G=0.7450	A=0.2550
1000Genomes	Europe	Sub	1006	G=0.9821	A=0.0179
1000Genomes	South Asian	Sub	978	G=0.877	A=0.123
1000Genomes	American	Sub	694	G=0.846	A=0.154
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.9574	A=0.0426
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.9875	A=0.0125
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.9908	A=0.0092
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.7294	A=0.2706
HapMap	Global	Study-wide	1890	G=0.8688	A=0.1312
HapMap	American	Sub	770	G=0.871	A=0.129
HapMap	African	Sub	690	G=0.901	A=0.099
HapMap	Asian	Sub	254	G=0.693	A=0.307
HapMap	Europe	Sub	176	G=0.983	A=0.017
Korean Genome Project	KOREAN	Study-wide	1832	G=0.7102	A=0.2898
Genome-wide autozygosity in Daghestan	Global	Study-wide	1132	G=0.9488	A=0.0512
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	G=0.955	A=0.045
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	G=0.993	A=0.007
Genome-wide autozygosity in Daghestan	Central Asia	Sub	120	G=0.908	A=0.092
Genome-wide autozygosity in Daghestan	Europe	Sub	108	G=0.981	A=0.019
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	G=0.85	A=0.15
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	G=0.97	A=0.03
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.994	A=0.006
Chileans	Chilean	Study-wide	626	G=0.778	A=0.222
Northern Sweden	ACPOP	Study-wide	600	G=0.955	A=0.045
Qatari	Global	Study-wide	216	G=0.972	A=0.028
A Vietnamese Genetic Variation Database	Global	Study-wide	212	G=0.816	A=0.184
SGDP_PRJ	Global	Study-wide	152	G=0.401	A=0.599
The Danish reference pan genome	Danish	Study-wide	40	G=0.97	A=0.03
Siberian	Global	Study-wide	20	G=0.30	A=0.70

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 6	NC_000006.12:g.151752183G>A
GRCh37.p13 chr 6	NC_000006.11:g.152073318G>A
ESR1 RefSeqGene (LRG_992)	NG_008493.2:g.100493G>A

Gene: ESR1, estrogen receptor 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ESR1 transcript variant 4	NM_001122742.2:c.-71+5017… NM_001122742.2:c.-71+50178G>A	N/A	Intron Variant
ESR1 transcript variant 8	NM_001385568.1:c.-71+5017… NM_001385568.1:c.-71+50178G>A	N/A	Intron Variant
ESR1 transcript variant 10	NM_001385570.1:c.-71+5017… NM_001385570.1:c.-71+50178G>A	N/A	Intron Variant
ESR1 transcript variant 1	NM_000125.4:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant 2	NM_001122740.2:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant 3	NM_001122741.2:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant 5	NM_001291230.2:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant 6	NM_001291241.2:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant 7	NM_001328100.2:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant 9	NM_001385569.1:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant 11	NM_001385571.1:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant 12	NM_001385572.1:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant X4	XM_011535543.3:c.-184-529… XM_011535543.3:c.-184-5297G>A	N/A	Intron Variant
ESR1 transcript variant X10	XM_011535547.3:c.-71+5017… XM_011535547.3:c.-71+50178G>A	N/A	Intron Variant
ESR1 transcript variant X2	XM_017010377.2:c.-71+5017… XM_017010377.2:c.-71+50178G>A	N/A	Intron Variant
ESR1 transcript variant X1	XM_017010378.2:c.-71+5017… XM_017010378.2:c.-71+50178G>A	N/A	Intron Variant
ESR1 transcript variant X7	XM_017010379.2:c.-71+5017… XM_017010379.2:c.-71+50178G>A	N/A	Intron Variant
ESR1 transcript variant X5	XM_017010380.2:c.-70-5566… XM_017010380.2:c.-70-55660G>A	N/A	Intron Variant
ESR1 transcript variant X6	XM_047418290.1:c.-71+5017… XM_047418290.1:c.-71+50178G>A	N/A	Intron Variant
ESR1 transcript variant X15	XM_047418295.1:c.-71+5017… XM_047418295.1:c.-71+50178G>A	N/A	Intron Variant
ESR1 transcript variant X17	XM_047418297.1:c.-71+5017… XM_047418297.1:c.-71+50178G>A	N/A	Intron Variant
ESR1 transcript variant X9	XM_011535545.3:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant X20	XM_011535549.3:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant X8	XM_017010381.2:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant X21	XM_017010383.2:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant X3	XM_047418289.1:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant X11	XM_047418291.1:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant X12	XM_047418292.1:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant X13	XM_047418293.1:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant X14	XM_047418294.1:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant X16	XM_047418296.1:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant X18	XM_047418298.1:c.	N/A	Genic Upstream Transcript Variant
ESR1 transcript variant X19	XM_047418299.1:c.	N/A	Genic Upstream Transcript Variant

Gene: LOC107986529, uncharacterized LOC107986529 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC107986529 transcript variant X1	XR_001743866.2:n.4073C>T	N/A	Non Coding Transcript Variant
LOC107986529 transcript variant X2	XR_007059818.1:n.4006C>T	N/A	Non Coding 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	G=	A
GRCh38.p14 chr 6	NC_000006.12:g.151752183=	NC_000006.12:g.151752183G>A
GRCh37.p13 chr 6	NC_000006.11:g.152073318=	NC_000006.11:g.152073318G>A
ESR1 RefSeqGene (LRG_992)	NG_008493.2:g.100493=	NG_008493.2:g.100493G>A
LOC107986529 transcript variant X1	XR_001743866.2:n.4073=	XR_001743866.2:n.4073C>T
LOC107986529 transcript variant X2	XR_007059818.1:n.4006=	XR_007059818.1:n.4006C>T
ESR1 transcript variant 4	NM_001122742.1:c.-71+50178=	NM_001122742.1:c.-71+50178G>A
ESR1 transcript variant 4	NM_001122742.2:c.-71+50178=	NM_001122742.2:c.-71+50178G>A
ESR1 transcript variant 8	NM_001385568.1:c.-71+50178=	NM_001385568.1:c.-71+50178G>A
ESR1 transcript variant 10	NM_001385570.1:c.-71+50178=	NM_001385570.1:c.-71+50178G>A
ESR1 transcript variant X4	XM_011535543.3:c.-184-5297=	XM_011535543.3:c.-184-5297G>A
ESR1 transcript variant X10	XM_011535547.3:c.-71+50178=	XM_011535547.3:c.-71+50178G>A
ESR1 transcript variant X2	XM_017010377.2:c.-71+50178=	XM_017010377.2:c.-71+50178G>A
ESR1 transcript variant X1	XM_017010378.2:c.-71+50178=	XM_017010378.2:c.-71+50178G>A
ESR1 transcript variant X7	XM_017010379.2:c.-71+50178=	XM_017010379.2:c.-71+50178G>A
ESR1 transcript variant X5	XM_017010380.2:c.-70-55660=	XM_017010380.2:c.-70-55660G>A
ESR1 transcript variant X6	XM_047418290.1:c.-71+50178=	XM_047418290.1:c.-71+50178G>A
ESR1 transcript variant X15	XM_047418295.1:c.-71+50178=	XM_047418295.1:c.-71+50178G>A
ESR1 transcript variant X17	XM_047418297.1:c.-71+50178=	XM_047418297.1:c.-71+50178G>A

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#.

67 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PERLEGEN	ss12673824	Dec 05, 2003 (119)
2	SC_SNP	ss12844313	Dec 05, 2003 (119)
3	SC_SNP	ss15753580	Feb 27, 2004 (120)
4	PERLEGEN	ss24049467	Sep 20, 2004 (123)
5	AFFY	ss66447168	Nov 30, 2006 (127)
6	PERLEGEN	ss68996201	May 17, 2007 (127)
7	AFFY	ss76233623	Dec 06, 2007 (129)
8	KRIBB_YJKIM	ss82567233	Dec 15, 2007 (130)
9	AFFY	ss172909330	Jul 04, 2010 (132)
10	1000GENOMES	ss211947864	Jul 14, 2010 (132)
11	1000GENOMES	ss222759868	Jul 14, 2010 (132)
12	1000GENOMES	ss233742090	Jul 15, 2010 (132)
13	1000GENOMES	ss240745619	Jul 15, 2010 (132)
14	GMI	ss279079924	May 04, 2012 (137)
15	ILLUMINA	ss481241029	May 04, 2012 (137)
16	ILLUMINA	ss485176588	May 04, 2012 (137)
17	ILLUMINA	ss534204411	Sep 08, 2015 (146)
18	TISHKOFF	ss559625503	Apr 25, 2013 (138)
19	SSMP	ss653967757	Apr 25, 2013 (138)
20	ILLUMINA	ss779845235	Sep 08, 2015 (146)
21	ILLUMINA	ss781432031	Sep 08, 2015 (146)
22	ILLUMINA	ss835322060	Sep 08, 2015 (146)
23	EVA-GONL	ss983662340	Aug 21, 2014 (142)
24	JMKIDD_LAB	ss1074156867	Aug 21, 2014 (142)
25	1000GENOMES	ss1322896255	Aug 21, 2014 (142)
26	HAMMER_LAB	ss1397475934	Sep 08, 2015 (146)
27	EVA_GENOME_DK	ss1581956965	Apr 01, 2015 (144)
28	EVA_DECODE	ss1593238305	Apr 01, 2015 (144)
29	EVA_UK10K_ALSPAC	ss1617032932	Apr 01, 2015 (144)
30	EVA_UK10K_TWINSUK	ss1660026965	Apr 01, 2015 (144)
31	EVA_SVP	ss1712911674	Apr 01, 2015 (144)
32	WEILL_CORNELL_DGM	ss1926905916	Feb 12, 2016 (147)
33	JJLAB	ss2024116288	Sep 14, 2016 (149)
34	USC_VALOUEV	ss2152307258	Dec 20, 2016 (150)
35	HUMAN_LONGEVITY	ss2289691721	Dec 20, 2016 (150)
36	ILLUMINA	ss2634530720	Nov 08, 2017 (151)
37	GRF	ss2707944514	Nov 08, 2017 (151)
38	GNOMAD	ss2846885967	Nov 08, 2017 (151)
39	SWEGEN	ss3000195472	Nov 08, 2017 (151)
40	ILLUMINA	ss3629690796	Oct 12, 2018 (152)
41	ILLUMINA	ss3632442979	Oct 12, 2018 (152)
42	ILLUMINA	ss3642527658	Oct 12, 2018 (152)
43	EGCUT_WGS	ss3668132140	Jul 13, 2019 (153)
44	EVA_DECODE	ss3718582170	Jul 13, 2019 (153)
45	ACPOP	ss3734117529	Jul 13, 2019 (153)
46	EVA	ss3765860901	Jul 13, 2019 (153)
47	KHV_HUMAN_GENOMES	ss3809021940	Jul 13, 2019 (153)
48	EVA	ss3830269323	Apr 26, 2020 (154)
49	SGDP_PRJ	ss3866036181	Apr 26, 2020 (154)
50	KRGDB	ss3913015610	Apr 26, 2020 (154)
51	KOGIC	ss3960368252	Apr 26, 2020 (154)
52	TOPMED	ss4727219912	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5180623644	Apr 26, 2021 (155)
54	1000G_HIGH_COVERAGE	ss5270896658	Oct 14, 2022 (156)
55	EVA	ss5315201910	Oct 14, 2022 (156)
56	EVA	ss5370007525	Oct 14, 2022 (156)
57	HUGCELL_USP	ss5468291063	Oct 14, 2022 (156)
58	EVA	ss5508762721	Oct 14, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5558114902	Oct 14, 2022 (156)
60	SANFORD_IMAGENETICS	ss5641805602	Oct 14, 2022 (156)
61	TOMMO_GENOMICS	ss5719703764	Oct 14, 2022 (156)
62	YY_MCH	ss5808092797	Oct 14, 2022 (156)
63	EVA	ss5843202165	Oct 14, 2022 (156)
64	EVA	ss5855647678	Oct 14, 2022 (156)
65	EVA	ss5886585759	Oct 14, 2022 (156)
66	EVA	ss5970754766	Oct 14, 2022 (156)
67	EVA	ss5970754767	Oct 14, 2022 (156)
68	1000Genomes	NC_000006.11 - 152073318	Oct 12, 2018 (152)
69	1000Genomes_30x	NC_000006.12 - 151752183	Oct 14, 2022 (156)
70	The Avon Longitudinal Study of Parents and Children	NC_000006.11 - 152073318	Oct 12, 2018 (152)
71	Chileans	NC_000006.11 - 152073318	Apr 26, 2020 (154)
72	Genome-wide autozygosity in Daghestan	NC_000006.10 - 152115011	Apr 26, 2020 (154)
73	Genetic variation in the Estonian population	NC_000006.11 - 152073318	Oct 12, 2018 (152)
74	The Danish reference pan genome	NC_000006.11 - 152073318	Apr 26, 2020 (154)
75	gnomAD - Genomes	NC_000006.12 - 151752183	Apr 26, 2021 (155)
76	Genome of the Netherlands Release 5	NC_000006.11 - 152073318	Apr 26, 2020 (154)
77	HapMap	NC_000006.12 - 151752183	Apr 26, 2020 (154)
78	KOREAN population from KRGDB	NC_000006.11 - 152073318	Apr 26, 2020 (154)
79	Korean Genome Project	NC_000006.12 - 151752183	Apr 26, 2020 (154)
80	Northern Sweden	NC_000006.11 - 152073318	Jul 13, 2019 (153)
81	Qatari	NC_000006.11 - 152073318	Apr 26, 2020 (154)
82	SGDP_PRJ	NC_000006.11 - 152073318	Apr 26, 2020 (154)
83	Siberian	NC_000006.11 - 152073318	Apr 26, 2020 (154)
84	8.3KJPN	NC_000006.11 - 152073318	Apr 26, 2021 (155)
85	14KJPN	NC_000006.12 - 151752183	Oct 14, 2022 (156)
86	TopMed	NC_000006.12 - 151752183	Apr 26, 2021 (155)
87	UK 10K study - Twins	NC_000006.11 - 152073318	Oct 12, 2018 (152)
88	A Vietnamese Genetic Variation Database	NC_000006.11 - 152073318	Jul 13, 2019 (153)
89	ALFA	NC_000006.12 - 151752183	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)
rs59632759	Feb 26, 2009 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
450301, ss66447168, ss76233623, ss172909330, ss211947864, ss279079924, ss485176588, ss1397475934, ss1593238305, ss1712911674	NC_000006.10:152115010:G:A	NC_000006.12:151752182:G:A	(self)
34788626, 19397049, 394759, 13870388, 8121904, 8633456, 20193004, 7402394, 8947846, 18053161, 4823612, 38592951, 19397049, 4317716, ss222759868, ss233742090, ss240745619, ss481241029, ss534204411, ss559625503, ss653967757, ss779845235, ss781432031, ss835322060, ss983662340, ss1074156867, ss1322896255, ss1581956965, ss1617032932, ss1660026965, ss1926905916, ss2024116288, ss2152307258, ss2634530720, ss2707944514, ss2846885967, ss3000195472, ss3629690796, ss3632442979, ss3642527658, ss3668132140, ss3734117529, ss3765860901, ss3830269323, ss3866036181, ss3913015610, ss5180623644, ss5315201910, ss5370007525, ss5508762721, ss5641805602, ss5843202165, ss5970754766, ss5970754767	NC_000006.11:152073317:G:A	NC_000006.12:151752182:G:A	(self)
45640837, 245624144, 3283525, 16746253, 53540868, 564597470, 9605961719, ss2289691721, ss3718582170, ss3809021940, ss3960368252, ss4727219912, ss5270896658, ss5468291063, ss5558114902, ss5719703764, ss5808092797, ss5855647678, ss5886585759	NC_000006.12:151752182:G:A	NC_000006.12:151752182:G:A	(self)
ss12844313	NT_023451.12:2046774:G:A	NC_000006.12:151752182:G:A	(self)
ss15753580	NT_025741.13:56228167:G:A	NC_000006.12:151752182:G:A	(self)
ss12673824, ss24049467, ss68996201, ss82567233	NT_025741.15:56242774:G:A	NC_000006.12:151752182:G:A	(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 rs9322330

PMID	Title	Author	Year	Journal
14740319	Matching strategies for genetic association studies in structured populations.	Hinds DA et al.	2004	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
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

rs9322330