Name: rs133437
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.

rs133437

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr22:35428022-35428038 (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(T)₉ / del(T)₆ / del(T)₅ / del(…
del(T)₉ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₉=0.000026 (7/264690, TOPMED)
delT=0.0462 (445/9630, ALFA)
delT=0.07 (3/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MCM5 : 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	9630	TTTTTTTTTTTTTTTTT=0.9279	TTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0462, TTTTTTTTTTTTTTTTTT=0.0259, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	0.917175	0.008282	0.074542	32
European	Sub	8598	TTTTTTTTTTTTTTTTT=0.9195	TTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0518, TTTTTTTTTTTTTTTTTT=0.0287, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	0.906726	0.009327	0.083947	32
African	Sub	226	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	6	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	220	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	72	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	64	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	54	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	404	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	72	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	204	TTTTTTTTTTTTTTTTT=0.990	TTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.010, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	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
TopMed	Global	Study-wide	264690	(T)₁₇=0.999974	del(T)₉=0.000026
Allele Frequency Aggregator	Total	Global	9630	(T)₁₇=0.9279	del(T)₉=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0462, dupT=0.0259, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	8598	(T)₁₇=0.9195	del(T)₉=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0518, dupT=0.0287, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	404	(T)₁₇=1.000	del(T)₉=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	African	Sub	226	(T)₁₇=1.000	del(T)₉=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	204	(T)₁₇=0.990	del(T)₉=0.000, del(T)₆=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.010, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	South Asian	Sub	72	(T)₁₇=1.00	del(T)₉=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Asian	Sub	72	(T)₁₇=1.00	del(T)₉=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	54	(T)₁₇=1.00	del(T)₉=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
The Danish reference pan genome	Danish	Study-wide	40	(T)₁₇=0.93	delT=0.07

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.35428030_35428038del
GRCh38.p14 chr 22	NC_000022.11:g.35428033_35428038del
GRCh38.p14 chr 22	NC_000022.11:g.35428034_35428038del
GRCh38.p14 chr 22	NC_000022.11:g.35428035_35428038del
GRCh38.p14 chr 22	NC_000022.11:g.35428036_35428038del
GRCh38.p14 chr 22	NC_000022.11:g.35428037_35428038del
GRCh38.p14 chr 22	NC_000022.11:g.35428038del
GRCh38.p14 chr 22	NC_000022.11:g.35428038dup
GRCh38.p14 chr 22	NC_000022.11:g.35428037_35428038dup
GRCh38.p14 chr 22	NC_000022.11:g.35428036_35428038dup
GRCh38.p14 chr 22	NC_000022.11:g.35428035_35428038dup
GRCh37.p13 chr 22	NC_000022.10:g.35824023_35824031del
GRCh37.p13 chr 22	NC_000022.10:g.35824026_35824031del
GRCh37.p13 chr 22	NC_000022.10:g.35824027_35824031del
GRCh37.p13 chr 22	NC_000022.10:g.35824028_35824031del
GRCh37.p13 chr 22	NC_000022.10:g.35824029_35824031del
GRCh37.p13 chr 22	NC_000022.10:g.35824030_35824031del
GRCh37.p13 chr 22	NC_000022.10:g.35824031del
GRCh37.p13 chr 22	NC_000022.10:g.35824031dup
GRCh37.p13 chr 22	NC_000022.10:g.35824030_35824031dup
GRCh37.p13 chr 22	NC_000022.10:g.35824029_35824031dup
GRCh37.p13 chr 22	NC_000022.10:g.35824028_35824031dup

Gene: MCM5, minichromosome maintenance complex component 5 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MCM5 transcript	NM_006739.4:c.	N/A	Genic Downstream Transcript Variant
MCM5 transcript variant X1	XM_006724242.5:c.2103+468… XM_006724242.5:c.2103+4689_2103+4697del	N/A	Intron Variant
MCM5 transcript variant X2	XM_047441366.1:c.2103+468… XM_047441366.1:c.2103+4689_2103+4697del	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	(T)₁₇=	del(T)₉	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄
GRCh38.p14 chr 22	NC_000022.11:g.35428022_35428038=	NC_000022.11:g.35428030_35428038del	NC_000022.11:g.35428033_35428038del	NC_000022.11:g.35428034_35428038del	NC_000022.11:g.35428035_35428038del	NC_000022.11:g.35428036_35428038del	NC_000022.11:g.35428037_35428038del	NC_000022.11:g.35428038del	NC_000022.11:g.35428038dup	NC_000022.11:g.35428037_35428038dup	NC_000022.11:g.35428036_35428038dup	NC_000022.11:g.35428035_35428038dup
GRCh37.p13 chr 22	NC_000022.10:g.35824015_35824031=	NC_000022.10:g.35824023_35824031del	NC_000022.10:g.35824026_35824031del	NC_000022.10:g.35824027_35824031del	NC_000022.10:g.35824028_35824031del	NC_000022.10:g.35824029_35824031del	NC_000022.10:g.35824030_35824031del	NC_000022.10:g.35824031del	NC_000022.10:g.35824031dup	NC_000022.10:g.35824030_35824031dup	NC_000022.10:g.35824029_35824031dup	NC_000022.10:g.35824028_35824031dup
MCM5 transcript variant X1	XM_006724242.5:c.2103+4681=	XM_006724242.5:c.2103+4689_2103+4697del	XM_006724242.5:c.2103+4692_2103+4697del	XM_006724242.5:c.2103+4693_2103+4697del	XM_006724242.5:c.2103+4694_2103+4697del	XM_006724242.5:c.2103+4695_2103+4697del	XM_006724242.5:c.2103+4696_2103+4697del	XM_006724242.5:c.2103+4697del	XM_006724242.5:c.2103+4697dup	XM_006724242.5:c.2103+4696_2103+4697dup	XM_006724242.5:c.2103+4695_2103+4697dup	XM_006724242.5:c.2103+4694_2103+4697dup
MCM5 transcript variant X2	XM_047441366.1:c.2103+4681=	XM_047441366.1:c.2103+4689_2103+4697del	XM_047441366.1:c.2103+4692_2103+4697del	XM_047441366.1:c.2103+4693_2103+4697del	XM_047441366.1:c.2103+4694_2103+4697del	XM_047441366.1:c.2103+4695_2103+4697del	XM_047441366.1:c.2103+4696_2103+4697del	XM_047441366.1:c.2103+4697del	XM_047441366.1:c.2103+4697dup	XM_047441366.1:c.2103+4696_2103+4697dup	XM_047441366.1:c.2103+4695_2103+4697dup	XM_047441366.1:c.2103+4694_2103+4697dup

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#.

34 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC	ss141262	Jun 24, 2000 (78)
2	EVA_GENOME_DK	ss1575833232	Apr 01, 2015 (144)
3	SWEGEN	ss3019294539	Nov 08, 2017 (151)
4	EVA_DECODE	ss3708189726	Jul 13, 2019 (153)
5	EVA_DECODE	ss3708189728	Jul 13, 2019 (153)
6	EVA_DECODE	ss3708189729	Jul 13, 2019 (153)
7	EVA_DECODE	ss3708189730	Jul 13, 2019 (153)
8	PACBIO	ss3788825650	Jul 13, 2019 (153)
9	EVA	ss3835989554	Apr 27, 2020 (154)
10	KOGIC	ss3983632038	Apr 27, 2020 (154)
11	KOGIC	ss3983632039	Apr 27, 2020 (154)
12	GNOMAD	ss4364509825	Apr 26, 2021 (155)
13	GNOMAD	ss4364509827	Apr 26, 2021 (155)
14	GNOMAD	ss4364509828	Apr 26, 2021 (155)
15	GNOMAD	ss4364509829	Apr 26, 2021 (155)
16	GNOMAD	ss4364509831	Apr 26, 2021 (155)
17	GNOMAD	ss4364509832	Apr 26, 2021 (155)
18	GNOMAD	ss4364509833	Apr 26, 2021 (155)
19	GNOMAD	ss4364509834	Apr 26, 2021 (155)
20	GNOMAD	ss4364509835	Apr 26, 2021 (155)
21	GNOMAD	ss4364509836	Apr 26, 2021 (155)
22	TOPMED	ss5109029333	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5232601063	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5232601064	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5232601065	Apr 26, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5311081836	Oct 16, 2022 (156)
27	HUGCELL_USP	ss5502925912	Oct 16, 2022 (156)
28	HUGCELL_USP	ss5502925913	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5502925914	Oct 16, 2022 (156)
30	TOMMO_GENOMICS	ss5793712913	Oct 16, 2022 (156)
31	TOMMO_GENOMICS	ss5793712914	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5793712915	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5793712916	Oct 16, 2022 (156)
34	YY_MCH	ss5818708794	Oct 16, 2022 (156)
35	The Danish reference pan genome	NC_000022.10 - 35824015	Apr 27, 2020 (154)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569818839 (NC_000022.11:35428021::T 10126/121278) Row 569818841 (NC_000022.11:35428021::TT 148/121374) Row 569818842 (NC_000022.11:35428021::TTT 0/121374)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569818839 (NC_000022.11:35428021::T 10126/121278) Row 569818841 (NC_000022.11:35428021::TT 148/121374) Row 569818842 (NC_000022.11:35428021::TTT 0/121374)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569818839 (NC_000022.11:35428021::T 10126/121278) Row 569818841 (NC_000022.11:35428021::TT 148/121374) Row 569818842 (NC_000022.11:35428021::TTT 0/121374)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569818839 (NC_000022.11:35428021::T 10126/121278) Row 569818841 (NC_000022.11:35428021::TT 148/121374) Row 569818842 (NC_000022.11:35428021::TTT 0/121374)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569818839 (NC_000022.11:35428021::T 10126/121278) Row 569818841 (NC_000022.11:35428021::TT 148/121374) Row 569818842 (NC_000022.11:35428021::TTT 0/121374)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569818839 (NC_000022.11:35428021::T 10126/121278) Row 569818841 (NC_000022.11:35428021::TT 148/121374) Row 569818842 (NC_000022.11:35428021::TTT 0/121374)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569818839 (NC_000022.11:35428021::T 10126/121278) Row 569818841 (NC_000022.11:35428021::TT 148/121374) Row 569818842 (NC_000022.11:35428021::TTT 0/121374)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569818839 (NC_000022.11:35428021::T 10126/121278) Row 569818841 (NC_000022.11:35428021::TT 148/121374) Row 569818842 (NC_000022.11:35428021::TTT 0/121374)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569818839 (NC_000022.11:35428021::T 10126/121278) Row 569818841 (NC_000022.11:35428021::TT 148/121374) Row 569818842 (NC_000022.11:35428021::TTT 0/121374)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 569818839 (NC_000022.11:35428021::T 10126/121278) Row 569818841 (NC_000022.11:35428021::TT 148/121374) Row 569818842 (NC_000022.11:35428021::TTT 0/121374)...	-	Apr 26, 2021 (155)
46	Korean Genome Project Submission ignored due to conflicting rows: Row 40010039 (NC_000022.11:35428022::T 68/1828) Row 40010040 (NC_000022.11:35428021:T: 356/1828)	-	Apr 27, 2020 (154)
47	Korean Genome Project Submission ignored due to conflicting rows: Row 40010039 (NC_000022.11:35428022::T 68/1828) Row 40010040 (NC_000022.11:35428021:T: 356/1828)	-	Apr 27, 2020 (154)
48	8.3KJPN Submission ignored due to conflicting rows: Row 90570370 (NC_000022.10:35824014:T: 1938/16656) Row 90570371 (NC_000022.10:35824014:TT: 31/16656) Row 90570372 (NC_000022.10:35824014::T 10/16656)	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 90570370 (NC_000022.10:35824014:T: 1938/16656) Row 90570371 (NC_000022.10:35824014:TT: 31/16656) Row 90570372 (NC_000022.10:35824014::T 10/16656)	-	Apr 26, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 90570370 (NC_000022.10:35824014:T: 1938/16656) Row 90570371 (NC_000022.10:35824014:TT: 31/16656) Row 90570372 (NC_000022.10:35824014::T 10/16656)	-	Apr 26, 2021 (155)
51	14KJPN Submission ignored due to conflicting rows: Row 127550017 (NC_000022.11:35428021:TT: 112/28166) Row 127550018 (NC_000022.11:35428021:T: 3359/28166) Row 127550019 (NC_000022.11:35428021:TTT: 4/28166)...	-	Oct 16, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 127550017 (NC_000022.11:35428021:TT: 112/28166) Row 127550018 (NC_000022.11:35428021:T: 3359/28166) Row 127550019 (NC_000022.11:35428021:TTT: 4/28166)...	-	Oct 16, 2022 (156)
53	14KJPN Submission ignored due to conflicting rows: Row 127550017 (NC_000022.11:35428021:TT: 112/28166) Row 127550018 (NC_000022.11:35428021:T: 3359/28166) Row 127550019 (NC_000022.11:35428021:TTT: 4/28166)...	-	Oct 16, 2022 (156)
54	14KJPN Submission ignored due to conflicting rows: Row 127550017 (NC_000022.11:35428021:TT: 112/28166) Row 127550018 (NC_000022.11:35428021:T: 3359/28166) Row 127550019 (NC_000022.11:35428021:TTT: 4/28166)...	-	Oct 16, 2022 (156)
55	TopMed	NC_000022.11 - 35428022	Apr 26, 2021 (155)
56	ALFA	NC_000022.11 - 35428022	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
384138280, ss4364509836, ss5109029333	NC_000022.11:35428021:TTTTTTTTT:	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
7160817138	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
7160817138	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3019294539	NC_000022.10:35824014:TTTTT:	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4364509835	NC_000022.11:35428021:TTTTT:	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
7160817138	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4364509834	NC_000022.11:35428021:TTTT:	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3708189726, ss4364509833, ss5793712915	NC_000022.11:35428021:TTT:	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
7160817138	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5232601064	NC_000022.10:35824014:TT:	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4364509832, ss5311081836, ss5502925913, ss5793712913	NC_000022.11:35428021:TT:	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7160817138	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3708189728	NC_000022.11:35428022:TT:	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
795433, ss1575833232, ss3788825650, ss3835989554, ss5232601063	NC_000022.10:35824014:T:	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3983632039, ss4364509831, ss5502925912, ss5793712914, ss5818708794	NC_000022.11:35428021:T:	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
7160817138	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3708189729	NC_000022.11:35428023:T:	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5232601065	NC_000022.10:35824014::T	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4364509825, ss5502925914, ss5793712916	NC_000022.11:35428021::T	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
7160817138	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3983632038	NC_000022.11:35428022::T	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3708189730	NC_000022.11:35428024::T	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss141262	NT_011520.12:15214600::T	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4364509827	NC_000022.11:35428021::TT	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
7160817138	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4364509828	NC_000022.11:35428021::TTT	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
7160817138	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4364509829	NC_000022.11:35428021::TTTT	NC_000022.11:35428021:TTTTTTTTTTTT… NC_000022.11:35428021:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(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 rs133437

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

rs133437