Name: rs746921769
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.

rs746921769

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:49832368-49832386 (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)₁₃ / del(A)₁₂ / del(A)₁₀ / d…
del(A)₁₃ / del(A)₁₂ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / delAAA / delAA / delA / dupA / dupAA / dup(A)₄ / dup(A)₅ / dup(A)₇ / dup(A)₈ / dup(A)₉ / dup(A)₁₃ / dup(A)₁₄
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₃=0.00000 (0/12902, ALFA)
del(A)₁₂=0.00000 (0/12902, ALFA)
del(A)₁₀=0.00000 (0/12902, ALFA) (+ 8 more)
del(A)₉=0.00000 (0/12902, ALFA)
del(A)₈=0.00000 (0/12902, ALFA)
del(A)₇=0.00000 (0/12902, ALFA)
delAA=0.00000 (0/12902, ALFA)
delA=0.00000 (0/12902, ALFA)
dupA=0.00000 (0/12902, ALFA)
dupAA=0.00000 (0/12902, ALFA)
dup(A)₄=0.00000 (0/12902, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	12902	AAAAAAAAAAAAAAAAAAA=1.00000	AAAAAA=0.00000, AAAAAAA=0.00000, AAAAAAAAA=0.00000, AAAAAAAAAA=0.00000, AAAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAAAA=0.00000	1.0	N/A
European	Sub	9612	AAAAAAAAAAAAAAAAAAA=1.0000	AAAAAA=0.0000, AAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1918	AAAAAAAAAAAAAAAAAAA=1.0000	AAAAAA=0.0000, AAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	62	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1856	AAAAAAAAAAAAAAAAAAA=1.0000	AAAAAA=0.0000, AAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	112	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAA=0.000, AAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
East Asian	Sub	86	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	26	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	130	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAA=0.000, AAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	596	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAA=0.000, AAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	94	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAA=0.00, AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	440	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAA=0.000, AAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	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
Allele Frequency Aggregator	Total	Global	12902	(A)₁₉=1.00000	del(A)₁₃=0.00000, del(A)₁₂=0.00000, del(A)₁₀=0.00000, del(A)₉=0.00000, del(A)₈=0.00000, del(A)₇=0.00000, delAA=0.00000, delA=0.00000, dupA=0.00000, dupAA=0.00000, dup(A)₄=0.00000
Allele Frequency Aggregator	European	Sub	9612	(A)₁₉=1.0000	del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	1918	(A)₁₉=1.0000	del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	596	(A)₁₉=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	440	(A)₁₉=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	130	(A)₁₉=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Asian	Sub	112	(A)₁₉=1.000	del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	South Asian	Sub	94	(A)₁₉=1.00	del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₄=0.00

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 22	NC_000022.11:g.49832374_49832386del
GRCh38.p14 chr 22	NC_000022.11:g.49832375_49832386del
GRCh38.p14 chr 22	NC_000022.11:g.49832377_49832386del
GRCh38.p14 chr 22	NC_000022.11:g.49832378_49832386del
GRCh38.p14 chr 22	NC_000022.11:g.49832379_49832386del
GRCh38.p14 chr 22	NC_000022.11:g.49832380_49832386del
GRCh38.p14 chr 22	NC_000022.11:g.49832384_49832386del
GRCh38.p14 chr 22	NC_000022.11:g.49832385_49832386del
GRCh38.p14 chr 22	NC_000022.11:g.49832386del
GRCh38.p14 chr 22	NC_000022.11:g.49832386dup
GRCh38.p14 chr 22	NC_000022.11:g.49832385_49832386dup
GRCh38.p14 chr 22	NC_000022.11:g.49832383_49832386dup
GRCh38.p14 chr 22	NC_000022.11:g.49832382_49832386dup
GRCh38.p14 chr 22	NC_000022.11:g.49832380_49832386dup
GRCh38.p14 chr 22	NC_000022.11:g.49832379_49832386dup
GRCh38.p14 chr 22	NC_000022.11:g.49832378_49832386dup
GRCh38.p14 chr 22	NC_000022.11:g.49832374_49832386dup
GRCh38.p14 chr 22	NC_000022.11:g.49832373_49832386dup
GRCh37.p13 chr 22	NC_000022.10:g.50226022_50226034del
GRCh37.p13 chr 22	NC_000022.10:g.50226023_50226034del
GRCh37.p13 chr 22	NC_000022.10:g.50226025_50226034del
GRCh37.p13 chr 22	NC_000022.10:g.50226026_50226034del
GRCh37.p13 chr 22	NC_000022.10:g.50226027_50226034del
GRCh37.p13 chr 22	NC_000022.10:g.50226028_50226034del
GRCh37.p13 chr 22	NC_000022.10:g.50226032_50226034del
GRCh37.p13 chr 22	NC_000022.10:g.50226033_50226034del
GRCh37.p13 chr 22	NC_000022.10:g.50226034del
GRCh37.p13 chr 22	NC_000022.10:g.50226034dup
GRCh37.p13 chr 22	NC_000022.10:g.50226033_50226034dup
GRCh37.p13 chr 22	NC_000022.10:g.50226031_50226034dup
GRCh37.p13 chr 22	NC_000022.10:g.50226030_50226034dup
GRCh37.p13 chr 22	NC_000022.10:g.50226028_50226034dup
GRCh37.p13 chr 22	NC_000022.10:g.50226027_50226034dup
GRCh37.p13 chr 22	NC_000022.10:g.50226026_50226034dup
GRCh37.p13 chr 22	NC_000022.10:g.50226022_50226034dup
GRCh37.p13 chr 22	NC_000022.10:g.50226021_50226034dup

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)₁₃	del(A)₁₂	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	delAAA	delAA	delA	dupA	dupAA	dup(A)₄	dup(A)₅	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₃	dup(A)₁₄
GRCh38.p14 chr 22	NC_000022.11:g.49832368_49832386=	NC_000022.11:g.49832374_49832386del	NC_000022.11:g.49832375_49832386del	NC_000022.11:g.49832377_49832386del	NC_000022.11:g.49832378_49832386del	NC_000022.11:g.49832379_49832386del	NC_000022.11:g.49832380_49832386del	NC_000022.11:g.49832384_49832386del	NC_000022.11:g.49832385_49832386del	NC_000022.11:g.49832386del	NC_000022.11:g.49832386dup	NC_000022.11:g.49832385_49832386dup	NC_000022.11:g.49832383_49832386dup	NC_000022.11:g.49832382_49832386dup	NC_000022.11:g.49832380_49832386dup	NC_000022.11:g.49832379_49832386dup	NC_000022.11:g.49832378_49832386dup	NC_000022.11:g.49832374_49832386dup	NC_000022.11:g.49832373_49832386dup
GRCh37.p13 chr 22	NC_000022.10:g.50226016_50226034=	NC_000022.10:g.50226022_50226034del	NC_000022.10:g.50226023_50226034del	NC_000022.10:g.50226025_50226034del	NC_000022.10:g.50226026_50226034del	NC_000022.10:g.50226027_50226034del	NC_000022.10:g.50226028_50226034del	NC_000022.10:g.50226032_50226034del	NC_000022.10:g.50226033_50226034del	NC_000022.10:g.50226034del	NC_000022.10:g.50226034dup	NC_000022.10:g.50226033_50226034dup	NC_000022.10:g.50226031_50226034dup	NC_000022.10:g.50226030_50226034dup	NC_000022.10:g.50226028_50226034dup	NC_000022.10:g.50226027_50226034dup	NC_000022.10:g.50226026_50226034dup	NC_000022.10:g.50226022_50226034dup	NC_000022.10:g.50226021_50226034dup

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#.

42 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3019488477	Nov 08, 2017 (151)
2	PACBIO	ss3788857042	Jul 13, 2019 (153)
3	KOGIC	ss3983880756	Apr 27, 2020 (154)
4	KOGIC	ss3983880757	Apr 27, 2020 (154)
5	KOGIC	ss3983880758	Apr 27, 2020 (154)
6	GNOMAD	ss4366434104	Apr 27, 2021 (155)
7	GNOMAD	ss4366434105	Apr 27, 2021 (155)
8	GNOMAD	ss4366434106	Apr 27, 2021 (155)
9	GNOMAD	ss4366434107	Apr 27, 2021 (155)
10	GNOMAD	ss4366434108	Apr 27, 2021 (155)
11	GNOMAD	ss4366434109	Apr 27, 2021 (155)
12	GNOMAD	ss4366434110	Apr 27, 2021 (155)
13	GNOMAD	ss4366434111	Apr 27, 2021 (155)
14	GNOMAD	ss4366434112	Apr 27, 2021 (155)
15	GNOMAD	ss4366434113	Apr 27, 2021 (155)
16	GNOMAD	ss4366434114	Apr 27, 2021 (155)
17	GNOMAD	ss4366434115	Apr 27, 2021 (155)
18	GNOMAD	ss4366434116	Apr 27, 2021 (155)
19	GNOMAD	ss4366434117	Apr 27, 2021 (155)
20	GNOMAD	ss4366434118	Apr 27, 2021 (155)
21	TOPMED	ss5112997925	Apr 27, 2021 (155)
22	TOPMED	ss5112997926	Apr 27, 2021 (155)
23	TOPMED	ss5112997927	Apr 27, 2021 (155)
24	TOPMED	ss5112997928	Apr 27, 2021 (155)
25	TOPMED	ss5112997929	Apr 27, 2021 (155)
26	TOPMED	ss5112997930	Apr 27, 2021 (155)
27	TOMMO_GENOMICS	ss5233154824	Apr 27, 2021 (155)
28	TOMMO_GENOMICS	ss5233154825	Apr 27, 2021 (155)
29	TOMMO_GENOMICS	ss5233154826	Apr 27, 2021 (155)
30	TOMMO_GENOMICS	ss5233154827	Apr 27, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5311502731	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5311502732	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5311502733	Oct 16, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5311502734	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5503304322	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5503304323	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5503304324	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5503304325	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5794445431	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5794445432	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5794445433	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5794445434	Oct 16, 2022 (156)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 573130475 (NC_000022.11:49832367::A 2238/75244) Row 573130476 (NC_000022.11:49832367::AA 8/75400) Row 573130477 (NC_000022.11:49832367::AAAA 3/75394)...	-	Apr 27, 2021 (155)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 40258757 (NC_000022.11:49832367:AA: 25/1824) Row 40258758 (NC_000022.11:49832368:A: 238/1824) Row 40258759 (NC_000022.11:49832369::A 185/1824)	-	Apr 27, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 40258757 (NC_000022.11:49832367:AA: 25/1824) Row 40258758 (NC_000022.11:49832368:A: 238/1824) Row 40258759 (NC_000022.11:49832369::A 185/1824)	-	Apr 27, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 40258757 (NC_000022.11:49832367:AA: 25/1824) Row 40258758 (NC_000022.11:49832368:A: 238/1824) Row 40258759 (NC_000022.11:49832369::A 185/1824)	-	Apr 27, 2020 (154)
61	8.3KJPN Submission ignored due to conflicting rows: Row 91124131 (NC_000022.10:50226015::AAAAAAA 4/16668) Row 91124132 (NC_000022.10:50226015:A: 35/16668) Row 91124133 (NC_000022.10:50226015:AAAAAAA: 2/16668)...	-	Apr 27, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 91124131 (NC_000022.10:50226015::AAAAAAA 4/16668) Row 91124132 (NC_000022.10:50226015:A: 35/16668) Row 91124133 (NC_000022.10:50226015:AAAAAAA: 2/16668)...	-	Apr 27, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 91124131 (NC_000022.10:50226015::AAAAAAA 4/16668) Row 91124132 (NC_000022.10:50226015:A: 35/16668) Row 91124133 (NC_000022.10:50226015:AAAAAAA: 2/16668)...	-	Apr 27, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 91124131 (NC_000022.10:50226015::AAAAAAA 4/16668) Row 91124132 (NC_000022.10:50226015:A: 35/16668) Row 91124133 (NC_000022.10:50226015:AAAAAAA: 2/16668)...	-	Apr 27, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 128282535 (NC_000022.11:49832367:A: 60/28120) Row 128282536 (NC_000022.11:49832367::AAAAA 11/28120) Row 128282537 (NC_000022.11:49832367:AAAAAAA: 3/28120)...	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 128282535 (NC_000022.11:49832367:A: 60/28120) Row 128282536 (NC_000022.11:49832367::AAAAA 11/28120) Row 128282537 (NC_000022.11:49832367:AAAAAAA: 3/28120)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 128282535 (NC_000022.11:49832367:A: 60/28120) Row 128282536 (NC_000022.11:49832367::AAAAA 11/28120) Row 128282537 (NC_000022.11:49832367:AAAAAAA: 3/28120)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 128282535 (NC_000022.11:49832367:A: 60/28120) Row 128282536 (NC_000022.11:49832367::AAAAA 11/28120) Row 128282537 (NC_000022.11:49832367:AAAAAAA: 3/28120)...	-	Oct 16, 2022 (156)
69	TopMed Submission ignored due to conflicting rows: Row 388106872 (NC_000022.11:49832367::AAAA 1/264690) Row 388106873 (NC_000022.11:49832367:AAAAAAA: 159/264690) Row 388106874 (NC_000022.11:49832367:AAAAAAAAA: 4/264690)...	-	Apr 27, 2021 (155)
70	TopMed Submission ignored due to conflicting rows: Row 388106872 (NC_000022.11:49832367::AAAA 1/264690) Row 388106873 (NC_000022.11:49832367:AAAAAAA: 159/264690) Row 388106874 (NC_000022.11:49832367:AAAAAAAAA: 4/264690)...	-	Apr 27, 2021 (155)
71	TopMed Submission ignored due to conflicting rows: Row 388106872 (NC_000022.11:49832367::AAAA 1/264690) Row 388106873 (NC_000022.11:49832367:AAAAAAA: 159/264690) Row 388106874 (NC_000022.11:49832367:AAAAAAAAA: 4/264690)...	-	Apr 27, 2021 (155)
72	TopMed Submission ignored due to conflicting rows: Row 388106872 (NC_000022.11:49832367::AAAA 1/264690) Row 388106873 (NC_000022.11:49832367:AAAAAAA: 159/264690) Row 388106874 (NC_000022.11:49832367:AAAAAAAAA: 4/264690)...	-	Apr 27, 2021 (155)
73	TopMed Submission ignored due to conflicting rows: Row 388106872 (NC_000022.11:49832367::AAAA 1/264690) Row 388106873 (NC_000022.11:49832367:AAAAAAA: 159/264690) Row 388106874 (NC_000022.11:49832367:AAAAAAAAA: 4/264690)...	-	Apr 27, 2021 (155)
74	TopMed Submission ignored due to conflicting rows: Row 388106872 (NC_000022.11:49832367::AAAA 1/264690) Row 388106873 (NC_000022.11:49832367:AAAAAAA: 159/264690) Row 388106874 (NC_000022.11:49832367:AAAAAAAAA: 4/264690)...	-	Apr 27, 2021 (155)
75	ALFA	NC_000022.11 - 49832368	Apr 27, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5112997930	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAA:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAA	(self)
6091684519	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAA	(self)
ss5112997929	NC_000022.11:49832367:AAAAAAAAAAAA:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAA	(self)
6091684519	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAA	(self)
ss4366434118, ss5112997928	NC_000022.11:49832367:AAAAAAAAAA:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
6091684519	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4366434117, ss5112997927	NC_000022.11:49832367:AAAAAAAAA:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
6091684519	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4366434116, ss5503304325	NC_000022.11:49832367:AAAAAAAA:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
6091684519	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3019488477, ss5233154826	NC_000022.10:50226015:AAAAAAA:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4366434115, ss5112997926, ss5311502734, ss5794445433	NC_000022.11:49832367:AAAAAAA:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
6091684519	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4366434114	NC_000022.11:49832367:AAA:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3983880756, ss4366434113, ss5311502733, ss5503304324	NC_000022.11:49832367:AA:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
6091684519	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3788857042, ss5233154825	NC_000022.10:50226015:A:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4366434112, ss5311502731, ss5503304322, ss5794445431	NC_000022.11:49832367:A:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
6091684519	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3983880757	NC_000022.11:49832368:A:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5233154827	NC_000022.10:50226015::A	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4366434104, ss5311502732, ss5503304323, ss5794445434	NC_000022.11:49832367::A	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
6091684519	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3983880758	NC_000022.11:49832369::A	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4366434105	NC_000022.11:49832367::AA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
6091684519	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4366434106, ss5112997925	NC_000022.11:49832367::AAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
6091684519	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4366434107, ss5794445432	NC_000022.11:49832367::AAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5233154824	NC_000022.10:50226015::AAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4366434108	NC_000022.11:49832367::AAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4366434109	NC_000022.11:49832367::AAAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4366434110	NC_000022.11:49832367::AAAAAAAAAAA… NC_000022.11:49832367::AAAAAAAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4366434111	NC_000022.11:49832367::AAAAAAAAAAA… NC_000022.11:49832367::AAAAAAAAAAAAAA	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2415251186	NC_000022.10:50226015:AAAAAAAA:	NC_000022.11:49832367:AAAAAAAAAAAA… NC_000022.11:49832367:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA

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

No publications for rs746921769

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

rs746921769