Name: rs57922305
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.

rs57922305

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:151818241-151818255 (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)₆ / del(A)₅ / del(A)₄ / delA…
del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dup(A)₆
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₅=0.3379 (1692/5008, 1000G)
delAAA=0.000 (0/590, ALFA)
delAA=0.000 (0/590, ALFA) (+ 3 more)
delA=0.000 (0/590, ALFA)
dupA=0.000 (0/590, ALFA)
dupAA=0.000 (0/590, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: AADAC : Intron Variant
AADACL2-AS1 : 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	HWEP
Total	Global	590	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
European	Sub	370	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	124	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	N/A
African American	Sub	120	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	16	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	12	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	6	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 2	Sub	44	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	N/A
South Asian	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other	Sub	26	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	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
1000Genomes	Global	Study-wide	5008	(A)₁₅=0.3379	delAA=0.6621
1000Genomes	African	Sub	1322	(A)₁₅=0.3056	delAA=0.6944
1000Genomes	East Asian	Sub	1008	(A)₁₅=0.5040	delAA=0.4960
1000Genomes	Europe	Sub	1006	(A)₁₅=0.2863	delAA=0.7137
1000Genomes	South Asian	Sub	978	(A)₁₅=0.299	delAA=0.701
1000Genomes	American	Sub	694	(A)₁₅=0.288	delAA=0.712
Allele Frequency Aggregator	Total	Global	590	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	European	Sub	370	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	African	Sub	124	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	44	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Other	Sub	26	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	16	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	6	(A)₁₅=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
Allele Frequency Aggregator	South Asian	Sub	4	(A)₁₅=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0

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 3	NC_000003.12:g.151818250_151818255del
GRCh38.p14 chr 3	NC_000003.12:g.151818251_151818255del
GRCh38.p14 chr 3	NC_000003.12:g.151818252_151818255del
GRCh38.p14 chr 3	NC_000003.12:g.151818253_151818255del
GRCh38.p14 chr 3	NC_000003.12:g.151818254_151818255del
GRCh38.p14 chr 3	NC_000003.12:g.151818255del
GRCh38.p14 chr 3	NC_000003.12:g.151818255dup
GRCh38.p14 chr 3	NC_000003.12:g.151818254_151818255dup
GRCh38.p14 chr 3	NC_000003.12:g.151818250_151818255dup
GRCh37.p13 chr 3	NC_000003.11:g.151536038_151536043del
GRCh37.p13 chr 3	NC_000003.11:g.151536039_151536043del
GRCh37.p13 chr 3	NC_000003.11:g.151536040_151536043del
GRCh37.p13 chr 3	NC_000003.11:g.151536041_151536043del
GRCh37.p13 chr 3	NC_000003.11:g.151536042_151536043del
GRCh37.p13 chr 3	NC_000003.11:g.151536043del
GRCh37.p13 chr 3	NC_000003.11:g.151536043dup
GRCh37.p13 chr 3	NC_000003.11:g.151536042_151536043dup
GRCh37.p13 chr 3	NC_000003.11:g.151536038_151536043dup

Gene: AADAC, arylacetamide deacetylase (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
AADAC transcript	NM_001086.3:c.361+662_361… NM_001086.3:c.361+662_361+667del	N/A	Intron Variant
AADAC transcript variant X1	XM_005247104.5:c.310+662_… XM_005247104.5:c.310+662_310+667del	N/A	Intron Variant

Gene: AADACL2-AS1, AADACL2 antisense RNA 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
AADACL2-AS1 transcript variant 1	NR_110202.1:n.	N/A	Intron Variant
AADACL2-AS1 transcript variant 2	NR_110203.1: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	(A)₁₅=	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dup(A)₆
GRCh38.p14 chr 3	NC_000003.12:g.151818241_151818255=	NC_000003.12:g.151818250_151818255del	NC_000003.12:g.151818251_151818255del	NC_000003.12:g.151818252_151818255del	NC_000003.12:g.151818253_151818255del	NC_000003.12:g.151818254_151818255del	NC_000003.12:g.151818255del	NC_000003.12:g.151818255dup	NC_000003.12:g.151818254_151818255dup	NC_000003.12:g.151818250_151818255dup
GRCh37.p13 chr 3	NC_000003.11:g.151536029_151536043=	NC_000003.11:g.151536038_151536043del	NC_000003.11:g.151536039_151536043del	NC_000003.11:g.151536040_151536043del	NC_000003.11:g.151536041_151536043del	NC_000003.11:g.151536042_151536043del	NC_000003.11:g.151536043del	NC_000003.11:g.151536043dup	NC_000003.11:g.151536042_151536043dup	NC_000003.11:g.151536038_151536043dup
AADAC transcript	NM_001086.2:c.361+653=	NM_001086.2:c.361+662_361+667del	NM_001086.2:c.361+663_361+667del	NM_001086.2:c.361+664_361+667del	NM_001086.2:c.361+665_361+667del	NM_001086.2:c.361+666_361+667del	NM_001086.2:c.361+667del	NM_001086.2:c.361+667dup	NM_001086.2:c.361+666_361+667dup	NM_001086.2:c.361+662_361+667dup
AADAC transcript	NM_001086.3:c.361+653=	NM_001086.3:c.361+662_361+667del	NM_001086.3:c.361+663_361+667del	NM_001086.3:c.361+664_361+667del	NM_001086.3:c.361+665_361+667del	NM_001086.3:c.361+666_361+667del	NM_001086.3:c.361+667del	NM_001086.3:c.361+667dup	NM_001086.3:c.361+666_361+667dup	NM_001086.3:c.361+662_361+667dup
AADAC transcript variant X1	XM_005247103.1:c.361+653=	XM_005247103.1:c.361+662_361+667del	XM_005247103.1:c.361+663_361+667del	XM_005247103.1:c.361+664_361+667del	XM_005247103.1:c.361+665_361+667del	XM_005247103.1:c.361+666_361+667del	XM_005247103.1:c.361+667del	XM_005247103.1:c.361+667dup	XM_005247103.1:c.361+666_361+667dup	XM_005247103.1:c.361+662_361+667dup
AADAC transcript variant X2	XM_005247104.1:c.310+653=	XM_005247104.1:c.310+662_310+667del	XM_005247104.1:c.310+663_310+667del	XM_005247104.1:c.310+664_310+667del	XM_005247104.1:c.310+665_310+667del	XM_005247104.1:c.310+666_310+667del	XM_005247104.1:c.310+667del	XM_005247104.1:c.310+667dup	XM_005247104.1:c.310+666_310+667dup	XM_005247104.1:c.310+662_310+667dup
AADAC transcript variant X1	XM_005247104.5:c.310+653=	XM_005247104.5:c.310+662_310+667del	XM_005247104.5:c.310+663_310+667del	XM_005247104.5:c.310+664_310+667del	XM_005247104.5:c.310+665_310+667del	XM_005247104.5:c.310+666_310+667del	XM_005247104.5:c.310+667del	XM_005247104.5:c.310+667dup	XM_005247104.5:c.310+666_310+667dup	XM_005247104.5:c.310+662_310+667dup

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#.

60 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80339677	Dec 14, 2007 (129)
2	HGSV	ss83738000	Aug 21, 2014 (142)
3	HUMANGENOME_JCVI	ss95335385	Feb 04, 2009 (130)
4	GMI	ss288433227	May 04, 2012 (137)
5	SSMP	ss663367489	Apr 01, 2015 (144)
6	1000GENOMES	ss1371158474	Aug 21, 2014 (142)
7	DDI	ss1536378079	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1703880086	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1703880127	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1710111886	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710111889	Apr 01, 2015 (144)
12	SYSTEMSBIOZJU	ss2625420233	Nov 08, 2017 (151)
13	SYSTEMSBIOZJU	ss2625420234	Nov 08, 2017 (151)
14	SWEGEN	ss2993424785	Nov 08, 2017 (151)
15	MCHAISSO	ss3064072745	Nov 08, 2017 (151)
16	MCHAISSO	ss3064936170	Nov 08, 2017 (151)
17	MCHAISSO	ss3065911847	Nov 08, 2017 (151)
18	BEROUKHIMLAB	ss3644138698	Oct 12, 2018 (152)
19	BIOINF_KMB_FNS_UNIBA	ss3645751282	Oct 12, 2018 (152)
20	URBANLAB	ss3647557778	Oct 12, 2018 (152)
21	EVA_DECODE	ss3710567043	Jul 13, 2019 (153)
22	EVA_DECODE	ss3710567044	Jul 13, 2019 (153)
23	EVA_DECODE	ss3710567045	Jul 13, 2019 (153)
24	EVA_DECODE	ss3710567046	Jul 13, 2019 (153)
25	EVA_DECODE	ss3710567047	Jul 13, 2019 (153)
26	EVA_DECODE	ss3710567048	Jul 13, 2019 (153)
27	ACPOP	ss3730475084	Jul 13, 2019 (153)
28	ACPOP	ss3730475085	Jul 13, 2019 (153)
29	PACBIO	ss3789989952	Jul 13, 2019 (153)
30	PACBIO	ss3794864560	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3804002501	Jul 13, 2019 (153)
32	EVA	ss3828146292	Apr 25, 2020 (154)
33	EVA	ss3837506138	Apr 25, 2020 (154)
34	EVA	ss3842937485	Apr 25, 2020 (154)
35	KOGIC	ss3952687674	Apr 25, 2020 (154)
36	KOGIC	ss3952687675	Apr 25, 2020 (154)
37	KOGIC	ss3952687676	Apr 25, 2020 (154)
38	KOGIC	ss3952687677	Apr 25, 2020 (154)
39	GNOMAD	ss4083297306	Apr 26, 2021 (155)
40	GNOMAD	ss4083297307	Apr 26, 2021 (155)
41	GNOMAD	ss4083297308	Apr 26, 2021 (155)
42	GNOMAD	ss4083297309	Apr 26, 2021 (155)
43	GNOMAD	ss4083297310	Apr 26, 2021 (155)
44	GNOMAD	ss4083297311	Apr 26, 2021 (155)
45	GNOMAD	ss4083297312	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5162226810	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5162226811	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5162226812	Apr 26, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5256525537	Oct 12, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5256525538	Oct 12, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5256525539	Oct 12, 2022 (156)
52	HUGCELL_USP	ss5455615572	Oct 12, 2022 (156)
53	HUGCELL_USP	ss5455615573	Oct 12, 2022 (156)
54	HUGCELL_USP	ss5455615574	Oct 12, 2022 (156)
55	TOMMO_GENOMICS	ss5695290852	Oct 12, 2022 (156)
56	TOMMO_GENOMICS	ss5695290853	Oct 12, 2022 (156)
57	TOMMO_GENOMICS	ss5695290854	Oct 12, 2022 (156)
58	TOMMO_GENOMICS	ss5695290855	Oct 12, 2022 (156)
59	EVA	ss5826672004	Oct 12, 2022 (156)
60	EVA	ss5826672005	Oct 12, 2022 (156)
61	1000Genomes	NC_000003.11 - 151536029	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 10035311 (NC_000003.11:151536029:A: 3006/3854) Row 10035312 (NC_000003.11:151536028:AAA: 223/3854)	-	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 10035311 (NC_000003.11:151536029:A: 3006/3854) Row 10035312 (NC_000003.11:151536028:AAA: 223/3854)	-	Oct 12, 2018 (152)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 127973410 (NC_000003.12:151818240::A 709/128252) Row 127973411 (NC_000003.12:151818240:A: 21056/128014) Row 127973412 (NC_000003.12:151818240:AA: 78541/128126)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 127973410 (NC_000003.12:151818240::A 709/128252) Row 127973411 (NC_000003.12:151818240:A: 21056/128014) Row 127973412 (NC_000003.12:151818240:AA: 78541/128126)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 127973410 (NC_000003.12:151818240::A 709/128252) Row 127973411 (NC_000003.12:151818240:A: 21056/128014) Row 127973412 (NC_000003.12:151818240:AA: 78541/128126)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 127973410 (NC_000003.12:151818240::A 709/128252) Row 127973411 (NC_000003.12:151818240:A: 21056/128014) Row 127973412 (NC_000003.12:151818240:AA: 78541/128126)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 127973410 (NC_000003.12:151818240::A 709/128252) Row 127973411 (NC_000003.12:151818240:A: 21056/128014) Row 127973412 (NC_000003.12:151818240:AA: 78541/128126)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 127973410 (NC_000003.12:151818240::A 709/128252) Row 127973411 (NC_000003.12:151818240:A: 21056/128014) Row 127973412 (NC_000003.12:151818240:AA: 78541/128126)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 127973410 (NC_000003.12:151818240::A 709/128252) Row 127973411 (NC_000003.12:151818240:A: 21056/128014) Row 127973412 (NC_000003.12:151818240:AA: 78541/128126)...	-	Apr 26, 2021 (155)
71	Korean Genome Project Submission ignored due to conflicting rows: Row 9065675 (NC_000003.12:151818241:AA: 744/1830) Row 9065676 (NC_000003.12:151818243::A 27/1830) Row 9065677 (NC_000003.12:151818240:AAA: 12/1830)...	-	Apr 25, 2020 (154)
72	Korean Genome Project Submission ignored due to conflicting rows: Row 9065675 (NC_000003.12:151818241:AA: 744/1830) Row 9065676 (NC_000003.12:151818243::A 27/1830) Row 9065677 (NC_000003.12:151818240:AAA: 12/1830)...	-	Apr 25, 2020 (154)
73	Korean Genome Project Submission ignored due to conflicting rows: Row 9065675 (NC_000003.12:151818241:AA: 744/1830) Row 9065676 (NC_000003.12:151818243::A 27/1830) Row 9065677 (NC_000003.12:151818240:AAA: 12/1830)...	-	Apr 25, 2020 (154)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 9065675 (NC_000003.12:151818241:AA: 744/1830) Row 9065676 (NC_000003.12:151818243::A 27/1830) Row 9065677 (NC_000003.12:151818240:AAA: 12/1830)...	-	Apr 25, 2020 (154)
75	Northern Sweden Submission ignored due to conflicting rows: Row 3759949 (NC_000003.11:151536028:AA: 362/580) Row 3759950 (NC_000003.11:151536028:A: 57/580)	-	Jul 13, 2019 (153)
76	Northern Sweden Submission ignored due to conflicting rows: Row 3759949 (NC_000003.11:151536028:AA: 362/580) Row 3759950 (NC_000003.11:151536028:A: 57/580)	-	Jul 13, 2019 (153)
77	8.3KJPN Submission ignored due to conflicting rows: Row 20196117 (NC_000003.11:151536028:AA: 6099/16758) Row 20196118 (NC_000003.11:151536028:A: 3426/16758) Row 20196119 (NC_000003.11:151536028::A 62/16758)	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 20196117 (NC_000003.11:151536028:AA: 6099/16758) Row 20196118 (NC_000003.11:151536028:A: 3426/16758) Row 20196119 (NC_000003.11:151536028::A 62/16758)	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 20196117 (NC_000003.11:151536028:AA: 6099/16758) Row 20196118 (NC_000003.11:151536028:A: 3426/16758) Row 20196119 (NC_000003.11:151536028::A 62/16758)	-	Apr 26, 2021 (155)
80	14KJPN Submission ignored due to conflicting rows: Row 29127956 (NC_000003.12:151818240:AA: 10201/28258) Row 29127957 (NC_000003.12:151818240:A: 5886/28258) Row 29127958 (NC_000003.12:151818240::A 109/28258)...	-	Oct 12, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 29127956 (NC_000003.12:151818240:AA: 10201/28258) Row 29127957 (NC_000003.12:151818240:A: 5886/28258) Row 29127958 (NC_000003.12:151818240::A 109/28258)...	-	Oct 12, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 29127956 (NC_000003.12:151818240:AA: 10201/28258) Row 29127957 (NC_000003.12:151818240:A: 5886/28258) Row 29127958 (NC_000003.12:151818240::A 109/28258)...	-	Oct 12, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 29127956 (NC_000003.12:151818240:AA: 10201/28258) Row 29127957 (NC_000003.12:151818240:A: 5886/28258) Row 29127958 (NC_000003.12:151818240::A 109/28258)...	-	Oct 12, 2022 (156)
84	UK 10K study - Twins Submission ignored due to conflicting rows: Row 10035311 (NC_000003.11:151536029:A: 2847/3708) Row 10035312 (NC_000003.11:151536028:AAA: 200/3708)	-	Oct 12, 2018 (152)
85	UK 10K study - Twins Submission ignored due to conflicting rows: Row 10035311 (NC_000003.11:151536029:A: 2847/3708) Row 10035312 (NC_000003.11:151536028:AAA: 200/3708)	-	Oct 12, 2018 (152)
86	ALFA	NC_000003.12 - 151818241	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)
rs59164532	Oct 14, 2011 (136)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4083297312	NC_000003.12:151818240:AAAAAA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss3710567048, ss4083297311	NC_000003.12:151818240:AAAAA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4083297310	NC_000003.12:151818240:AAAA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3710567047	NC_000003.12:151818241:AAAA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss1703880086, ss1703880127, ss5826672005	NC_000003.11:151536028:AAA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3065911847, ss3952687676, ss4083297309, ss5695290855	NC_000003.12:151818240:AAA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
3911638480	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3710567046	NC_000003.12:151818242:AAA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss83738000	NC_000003.9:153018739:AA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
18014552, ss663367489, ss1371158474, ss1536378079, ss2625420233, ss2993424785, ss3644138698, ss3730475084, ss3789989952, ss3794864560, ss3828146292, ss3837506138, ss5162226810, ss5826672004	NC_000003.11:151536028:AA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1710111886, ss1710111889	NC_000003.11:151536029:AA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3064072745, ss3064936170, ss3645751282, ss3804002501, ss3842937485, ss4083297308, ss5256525537, ss5455615572, ss5695290852	NC_000003.12:151818240:AA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
3911638480	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3952687674	NC_000003.12:151818241:AA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3710567045	NC_000003.12:151818243:AA:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss80339677	NC_000003.9:153018740:A:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss288433227	NC_000003.10:153018718:A:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3730475085, ss5162226811	NC_000003.11:151536028:A:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss2625420234	NC_000003.11:151536029:A:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3647557778, ss4083297307, ss5256525538, ss5455615573, ss5695290853	NC_000003.12:151818240:A:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
3911638480	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3952687677	NC_000003.12:151818242:A:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3710567044	NC_000003.12:151818244:A:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss95335385	NT_005612.16:58031188:A:	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5162226812	NC_000003.11:151536028::A	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4083297306, ss5256525539, ss5455615574, ss5695290854	NC_000003.12:151818240::A	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
3911638480	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3952687675	NC_000003.12:151818243::A	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
3911638480	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3710567043	NC_000003.12:151818245::AAAAAA	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3409277397	NC_000003.12:151818240::AA	NC_000003.12:151818240:AAAAAAAAAAA… NC_000003.12:151818240:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA

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

No publications for rs57922305

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

rs57922305