Name: rs9322172
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.

rs9322172

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:149280932-149280950 (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: del(A)₉ / del(A)₆ / del(A)₅ / del(…
del(A)₉ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dup(A)₆
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₉=0.000 (0/334, ALFA)
del(A)₄=0.000 (0/334, ALFA)
delAAA=0.000 (0/334, ALFA) (+ 3 more)
delAA=0.000 (0/334, ALFA)
delA=0.000 (0/334, ALFA)
dupA=0.000 (0/334, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TAB2 : 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	334	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	304	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	6	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	6	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Asian	Sub	4	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	6	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	4	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	10	AAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A

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
Allele Frequency Aggregator	Total	Global	334	(A)₁₉=1.000	del(A)₉=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	European	Sub	304	(A)₁₉=1.000	del(A)₉=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	Other	Sub	10	(A)₁₉=1.0	del(A)₉=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	Latin American 2	Sub	6	(A)₁₉=1.0	del(A)₉=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	African	Sub	6	(A)₁₉=1.0	del(A)₉=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	South Asian	Sub	4	(A)₁₉=1.0	del(A)₉=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	Asian	Sub	4	(A)₁₉=1.0	del(A)₉=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₁₉=0	del(A)₉=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0

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.149280942_149280950del
GRCh38.p14 chr 6	NC_000006.12:g.149280945_149280950del
GRCh38.p14 chr 6	NC_000006.12:g.149280946_149280950del
GRCh38.p14 chr 6	NC_000006.12:g.149280947_149280950del
GRCh38.p14 chr 6	NC_000006.12:g.149280948_149280950del
GRCh38.p14 chr 6	NC_000006.12:g.149280949_149280950del
GRCh38.p14 chr 6	NC_000006.12:g.149280950del
GRCh38.p14 chr 6	NC_000006.12:g.149280950dup
GRCh38.p14 chr 6	NC_000006.12:g.149280949_149280950dup
GRCh38.p14 chr 6	NC_000006.12:g.149280945_149280950dup
GRCh37.p13 chr 6	NC_000006.11:g.149602078_149602086del
GRCh37.p13 chr 6	NC_000006.11:g.149602081_149602086del
GRCh37.p13 chr 6	NC_000006.11:g.149602082_149602086del
GRCh37.p13 chr 6	NC_000006.11:g.149602083_149602086del
GRCh37.p13 chr 6	NC_000006.11:g.149602084_149602086del
GRCh37.p13 chr 6	NC_000006.11:g.149602085_149602086del
GRCh37.p13 chr 6	NC_000006.11:g.149602086del
GRCh37.p13 chr 6	NC_000006.11:g.149602086dup
GRCh37.p13 chr 6	NC_000006.11:g.149602085_149602086dup
GRCh37.p13 chr 6	NC_000006.11:g.149602081_149602086dup
TAB2 RefSeqGene	NG_021386.2:g.68019_68027del
TAB2 RefSeqGene	NG_021386.2:g.68022_68027del
TAB2 RefSeqGene	NG_021386.2:g.68023_68027del
TAB2 RefSeqGene	NG_021386.2:g.68024_68027del
TAB2 RefSeqGene	NG_021386.2:g.68025_68027del
TAB2 RefSeqGene	NG_021386.2:g.68026_68027del
TAB2 RefSeqGene	NG_021386.2:g.68027del
TAB2 RefSeqGene	NG_021386.2:g.68027dup
TAB2 RefSeqGene	NG_021386.2:g.68026_68027dup
TAB2 RefSeqGene	NG_021386.2:g.68022_68027dup

Gene: TAB2, TGF-beta activated kinase 1 (MAP3K7) binding protein 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TAB2 transcript variant 4	NM_001292035.3:c.6+62166_… NM_001292035.3:c.6+62166_6+62174del	N/A	Intron Variant
TAB2 transcript variant 3	NM_001292034.3:c.	N/A	Genic Upstream Transcript Variant
TAB2 transcript variant 6	NM_001369506.1:c.	N/A	Genic Upstream Transcript Variant
TAB2 transcript variant 1	NM_015093.6:c.	N/A	Genic Upstream Transcript Variant
TAB2 transcript variant 5	NR_125861.2:n.	N/A	Genic Downstream Transcript Variant
TAB2 transcript variant X7	XM_011535633.3:c.	N/A	Genic Upstream Transcript Variant
TAB2 transcript variant X6	XM_017010592.3:c.	N/A	Genic Upstream Transcript Variant
TAB2 transcript variant X1	XM_047418485.1:c.	N/A	Genic Upstream Transcript Variant
TAB2 transcript variant X2	XM_047418486.1:c.	N/A	Genic Upstream Transcript Variant
TAB2 transcript variant X3	XM_047418487.1:c.	N/A	Genic Upstream Transcript Variant
TAB2 transcript variant X4	XM_047418488.1:c.	N/A	Genic Upstream Transcript Variant
TAB2 transcript variant X5	XM_047418489.1:c.	N/A	Genic Upstream Transcript Variant
TAB2 transcript variant X8	XM_047418490.1:c.	N/A	Genic Upstream 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	(A)₁₉=	del(A)₉	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dup(A)₆
GRCh38.p14 chr 6	NC_000006.12:g.149280932_149280950=	NC_000006.12:g.149280942_149280950del	NC_000006.12:g.149280945_149280950del	NC_000006.12:g.149280946_149280950del	NC_000006.12:g.149280947_149280950del	NC_000006.12:g.149280948_149280950del	NC_000006.12:g.149280949_149280950del	NC_000006.12:g.149280950del	NC_000006.12:g.149280950dup	NC_000006.12:g.149280949_149280950dup	NC_000006.12:g.149280945_149280950dup
GRCh37.p13 chr 6	NC_000006.11:g.149602068_149602086=	NC_000006.11:g.149602078_149602086del	NC_000006.11:g.149602081_149602086del	NC_000006.11:g.149602082_149602086del	NC_000006.11:g.149602083_149602086del	NC_000006.11:g.149602084_149602086del	NC_000006.11:g.149602085_149602086del	NC_000006.11:g.149602086del	NC_000006.11:g.149602086dup	NC_000006.11:g.149602085_149602086dup	NC_000006.11:g.149602081_149602086dup
TAB2 RefSeqGene	NG_021386.2:g.68009_68027=	NG_021386.2:g.68019_68027del	NG_021386.2:g.68022_68027del	NG_021386.2:g.68023_68027del	NG_021386.2:g.68024_68027del	NG_021386.2:g.68025_68027del	NG_021386.2:g.68026_68027del	NG_021386.2:g.68027del	NG_021386.2:g.68027dup	NG_021386.2:g.68026_68027dup	NG_021386.2:g.68022_68027dup
TAB2 transcript variant 4	NM_001292035.3:c.6+62156=	NM_001292035.3:c.6+62166_6+62174del	NM_001292035.3:c.6+62169_6+62174del	NM_001292035.3:c.6+62170_6+62174del	NM_001292035.3:c.6+62171_6+62174del	NM_001292035.3:c.6+62172_6+62174del	NM_001292035.3:c.6+62173_6+62174del	NM_001292035.3:c.6+62174del	NM_001292035.3:c.6+62174dup	NM_001292035.3:c.6+62173_6+62174dup	NM_001292035.3:c.6+62169_6+62174dup

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#.

53 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42786267	Apr 25, 2013 (144)
2	ABI	ss42883879	Mar 15, 2016 (147)
3	HUMANGENOME_JCVI	ss95445364	Dec 03, 2013 (144)
4	HUMANGENOME_JCVI	ss98462442	Dec 05, 2013 (138)
5	GMI	ss288808484	May 04, 2012 (137)
6	PJP	ss295313201	May 09, 2011 (137)
7	PJP	ss295313202	May 09, 2011 (138)
8	EVA_UK10K_ALSPAC	ss1705418233	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1705418399	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710300106	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710300108	Apr 01, 2015 (144)
12	SYSTEMSBIOZJU	ss2626542325	Nov 08, 2017 (151)
13	SWEGEN	ss3000164791	Nov 08, 2017 (151)
14	MCHAISSO	ss3065111131	Nov 08, 2017 (151)
15	MCHAISSO	ss3065111132	Nov 08, 2017 (151)
16	URBANLAB	ss3648496956	Oct 12, 2018 (152)
17	EVA_DECODE	ss3718544163	Jul 13, 2019 (153)
18	EVA_DECODE	ss3718544164	Jul 13, 2019 (153)
19	EVA_DECODE	ss3718544165	Jul 13, 2019 (153)
20	EVA_DECODE	ss3718544166	Jul 13, 2019 (153)
21	EVA_DECODE	ss3718544167	Jul 13, 2019 (153)
22	PACBIO	ss3785655068	Jul 13, 2019 (153)
23	PACBIO	ss3785655069	Jul 13, 2019 (153)
24	PACBIO	ss3790976743	Jul 13, 2019 (153)
25	PACBIO	ss3790976744	Jul 13, 2019 (153)
26	PACBIO	ss3795856139	Jul 13, 2019 (153)
27	EVA	ss3830258511	Apr 26, 2020 (154)
28	GNOMAD	ss4153809761	Apr 26, 2021 (155)
29	GNOMAD	ss4153809762	Apr 26, 2021 (155)
30	GNOMAD	ss4153809763	Apr 26, 2021 (155)
31	GNOMAD	ss4153809764	Apr 26, 2021 (155)
32	GNOMAD	ss4153809765	Apr 26, 2021 (155)
33	GNOMAD	ss4153809766	Apr 26, 2021 (155)
34	GNOMAD	ss4153809767	Apr 26, 2021 (155)
35	GNOMAD	ss4153809768	Apr 26, 2021 (155)
36	GNOMAD	ss4153809769	Apr 26, 2021 (155)
37	GNOMAD	ss4153809770	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5180539650	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5180539651	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5180539652	Apr 26, 2021 (155)
41	1000G_HIGH_COVERAGE	ss5270829669	Oct 13, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5270829670	Oct 13, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5270829671	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5468230814	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5468230815	Oct 13, 2022 (156)
46	HUGCELL_USP	ss5468230816	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5719595506	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5719595507	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5719595508	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5719595509	Oct 13, 2022 (156)
51	EVA	ss5843175719	Oct 13, 2022 (156)
52	EVA	ss5843175720	Oct 13, 2022 (156)
53	EVA	ss5886511481	Oct 13, 2022 (156)
54	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 19354064 (NC_000006.11:149602068:A: 3290/3854) Row 19354065 (NC_000006.11:149602067:AAA: 504/3854)	-	Oct 12, 2018 (152)
55	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 19354064 (NC_000006.11:149602068:A: 3290/3854) Row 19354065 (NC_000006.11:149602067:AAA: 504/3854)	-	Oct 12, 2018 (152)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245106883 (NC_000006.12:149280931::A 12/105330) Row 245106884 (NC_000006.12:149280931::AA 3/105356) Row 245106885 (NC_000006.12:149280931::AAAAAA 1/105360)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245106883 (NC_000006.12:149280931::A 12/105330) Row 245106884 (NC_000006.12:149280931::AA 3/105356) Row 245106885 (NC_000006.12:149280931::AAAAAA 1/105360)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245106883 (NC_000006.12:149280931::A 12/105330) Row 245106884 (NC_000006.12:149280931::AA 3/105356) Row 245106885 (NC_000006.12:149280931::AAAAAA 1/105360)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245106883 (NC_000006.12:149280931::A 12/105330) Row 245106884 (NC_000006.12:149280931::AA 3/105356) Row 245106885 (NC_000006.12:149280931::AAAAAA 1/105360)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245106883 (NC_000006.12:149280931::A 12/105330) Row 245106884 (NC_000006.12:149280931::AA 3/105356) Row 245106885 (NC_000006.12:149280931::AAAAAA 1/105360)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245106883 (NC_000006.12:149280931::A 12/105330) Row 245106884 (NC_000006.12:149280931::AA 3/105356) Row 245106885 (NC_000006.12:149280931::AAAAAA 1/105360)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245106883 (NC_000006.12:149280931::A 12/105330) Row 245106884 (NC_000006.12:149280931::AA 3/105356) Row 245106885 (NC_000006.12:149280931::AAAAAA 1/105360)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245106883 (NC_000006.12:149280931::A 12/105330) Row 245106884 (NC_000006.12:149280931::AA 3/105356) Row 245106885 (NC_000006.12:149280931::AAAAAA 1/105360)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245106883 (NC_000006.12:149280931::A 12/105330) Row 245106884 (NC_000006.12:149280931::AA 3/105356) Row 245106885 (NC_000006.12:149280931::AAAAAA 1/105360)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245106883 (NC_000006.12:149280931::A 12/105330) Row 245106884 (NC_000006.12:149280931::AA 3/105356) Row 245106885 (NC_000006.12:149280931::AAAAAA 1/105360)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 38508957 (NC_000006.11:149602067:AA: 8222/16648) Row 38508958 (NC_000006.11:149602067:A: 5874/16648) Row 38508959 (NC_000006.11:149602067:AAA: 27/16648)	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 38508957 (NC_000006.11:149602067:AA: 8222/16648) Row 38508958 (NC_000006.11:149602067:A: 5874/16648) Row 38508959 (NC_000006.11:149602067:AAA: 27/16648)	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 38508957 (NC_000006.11:149602067:AA: 8222/16648) Row 38508958 (NC_000006.11:149602067:A: 5874/16648) Row 38508959 (NC_000006.11:149602067:AAA: 27/16648)	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 53432610 (NC_000006.12:149280931:AA: 14739/28066) Row 53432611 (NC_000006.12:149280931:A: 10479/28066) Row 53432612 (NC_000006.12:149280931:AAA: 47/28066)...	-	Oct 13, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 53432610 (NC_000006.12:149280931:AA: 14739/28066) Row 53432611 (NC_000006.12:149280931:A: 10479/28066) Row 53432612 (NC_000006.12:149280931:AAA: 47/28066)...	-	Oct 13, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 53432610 (NC_000006.12:149280931:AA: 14739/28066) Row 53432611 (NC_000006.12:149280931:A: 10479/28066) Row 53432612 (NC_000006.12:149280931:AAA: 47/28066)...	-	Oct 13, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 53432610 (NC_000006.12:149280931:AA: 14739/28066) Row 53432611 (NC_000006.12:149280931:A: 10479/28066) Row 53432612 (NC_000006.12:149280931:AAA: 47/28066)...	-	Oct 13, 2022 (156)
73	UK 10K study - Twins Submission ignored due to conflicting rows: Row 19354064 (NC_000006.11:149602068:A: 3119/3708) Row 19354065 (NC_000006.11:149602067:AAA: 532/3708)	-	Oct 12, 2018 (152)
74	UK 10K study - Twins Submission ignored due to conflicting rows: Row 19354064 (NC_000006.11:149602068:A: 3119/3708) Row 19354065 (NC_000006.11:149602067:AAA: 532/3708)	-	Oct 12, 2018 (152)
75	ALFA	NC_000006.12 - 149280932	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)
rs33985916	May 23, 2006 (127)
rs67384567	May 04, 2012 (137)
rs67384568	Feb 27, 2009 (130)
rs67441069	Apr 25, 2013 (138)
rs71554438	Dec 02, 2009 (131)
rs71781067	Oct 16, 2011 (136)
rs374641513	Jul 01, 2015 (144)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4153809770	NC_000006.12:149280931:AAAAAAAAA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
907595227	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4153809769	NC_000006.12:149280931:AAAAAA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3718544167, ss4153809768	NC_000006.12:149280931:AAAAA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4153809767	NC_000006.12:149280931:AAAA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
907595227	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3718544166	NC_000006.12:149280932:AAAA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss1705418233, ss1705418399, ss3000164791, ss3785655068, ss3790976743, ss5180539652, ss5843175720	NC_000006.11:149602067:AAA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3065111131, ss4153809766, ss5270829669, ss5468230814, ss5719595508	NC_000006.12:149280931:AAA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
907595227	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3718544165	NC_000006.12:149280933:AAA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss288808484	NC_000006.10:149643760:AA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss2626542325, ss3785655069, ss3790976744, ss3795856139, ss3830258511, ss5180539650, ss5843175719	NC_000006.11:149602067:AA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss1710300106, ss1710300108	NC_000006.11:149602068:AA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3065111132, ss3648496956, ss4153809765, ss5270829670, ss5468230815, ss5719595506, ss5886511481	NC_000006.12:149280931:AA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
907595227	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3718544164	NC_000006.12:149280934:AA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss42883879, ss98462442	NT_025741.15:53771541:AA:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss295313201	NC_000006.10:149643760:A:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss295313202	NC_000006.10:149643778:A:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5180539651	NC_000006.11:149602067:A:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
	NC_000006.11:149602068:A:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4153809764, ss5270829671, ss5468230816, ss5719595507	NC_000006.12:149280931:A:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
907595227	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3718544163	NC_000006.12:149280935:A:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss42883879, ss98462442	NT_025741.15:53771541:AA:A	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss42786267, ss95445364	NT_025741.15:53771542:A:	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4153809761	NC_000006.12:149280931::A	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
907595227	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4153809762, ss5719595509	NC_000006.12:149280931::AA	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4153809763	NC_000006.12:149280931::AAAAAA	NC_000006.12:149280931:AAAAAAAAAAA… NC_000006.12:149280931:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs9322172

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

rs9322172