Name: rs371884745
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.

rs371884745

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:37792705-37792721 (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: delTTT / delTT / delT / dupT / dup…
delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₁₀ / ins(T)₄₆
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.3053 (2142/7016, ALFA)
dupT=0.3560 (1783/5008, 1000G)
dupT=0.42 (17/40, GENOME_DK) (+ 1 more)
dupT=0.1 (1/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC105376037 : 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	7016	TTTTTTTTTTTTTTTTT=0.6924	TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0010, TTTTTTTTTTTTTTTTTT=0.3053, TTTTTTTTTTTTTTTTTTT=0.0011, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0001, TTTTTTTTTTTTTTTTTTTT=0.0000	0.553265	0.164089	0.282646	32
European	Sub	5956	TTTTTTTTTTTTTTTTT=0.6382	TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTTTT=0.3593, TTTTTTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTTTTTT=0.0000	0.473844	0.193385	0.332771	32
African	Sub	678	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	28	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	650	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	62	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	52	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	22	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	134	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	28	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	136	TTTTTTTTTTTTTTTTT=0.978	TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.015, TTTTTTTTTTTTTTTTTTT=0.007, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	0.985075	0.0	0.014925	0

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	7016	(T)₁₇=0.6924	delTT=0.0000, delT=0.0010, dupT=0.3053, dupTT=0.0011, dupTTT=0.0000, ins(T)₄₆=0.0001
Allele Frequency Aggregator	European	Sub	5956	(T)₁₇=0.6382	delTT=0.0000, delT=0.0012, dupT=0.3593, dupTT=0.0012, dupTTT=0.0000, ins(T)₄₆=0.0002
Allele Frequency Aggregator	African	Sub	678	(T)₁₇=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, ins(T)₄₆=0.000
Allele Frequency Aggregator	Other	Sub	136	(T)₁₇=0.978	delTT=0.000, delT=0.000, dupT=0.015, dupTT=0.007, dupTTT=0.000, ins(T)₄₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	134	(T)₁₇=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, ins(T)₄₆=0.000
Allele Frequency Aggregator	Asian	Sub	62	(T)₁₇=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, ins(T)₄₆=0.00
Allele Frequency Aggregator	South Asian	Sub	28	(T)₁₇=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, ins(T)₄₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	22	(T)₁₇=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, ins(T)₄₆=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.3560
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.3313
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.2123
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.4851
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.335
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.454
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.42
KOREAN population from KRGDB	KOREAN	Study-wide	8	- No frequency provided	dupT=0.1

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 9	NC_000009.12:g.37792719_37792721del
GRCh38.p14 chr 9	NC_000009.12:g.37792720_37792721del
GRCh38.p14 chr 9	NC_000009.12:g.37792721del
GRCh38.p14 chr 9	NC_000009.12:g.37792721dup
GRCh38.p14 chr 9	NC_000009.12:g.37792720_37792721dup
GRCh38.p14 chr 9	NC_000009.12:g.37792719_37792721dup
GRCh38.p14 chr 9	NC_000009.12:g.37792712_37792721dup
GRCh38.p14 chr 9	NC_000009.12:g.37792721_37792722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 9	NC_000009.11:g.37792716_37792718del
GRCh37.p13 chr 9	NC_000009.11:g.37792717_37792718del
GRCh37.p13 chr 9	NC_000009.11:g.37792718del
GRCh37.p13 chr 9	NC_000009.11:g.37792718dup
GRCh37.p13 chr 9	NC_000009.11:g.37792717_37792718dup
GRCh37.p13 chr 9	NC_000009.11:g.37792716_37792718dup
GRCh37.p13 chr 9	NC_000009.11:g.37792709_37792718dup
GRCh37.p13 chr 9	NC_000009.11:g.37792718_37792719insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: LOC105376037, uncharacterized LOC105376037 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105376037 transcript	XR_929599.3: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	(T)₁₇=	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₁₀	ins(T)₄₆
GRCh38.p14 chr 9	NC_000009.12:g.37792705_37792721=	NC_000009.12:g.37792719_37792721del	NC_000009.12:g.37792720_37792721del	NC_000009.12:g.37792721del	NC_000009.12:g.37792721dup	NC_000009.12:g.37792720_37792721dup	NC_000009.12:g.37792719_37792721dup	NC_000009.12:g.37792712_37792721dup	NC_000009.12:g.37792721_37792722insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 9	NC_000009.11:g.37792702_37792718=	NC_000009.11:g.37792716_37792718del	NC_000009.11:g.37792717_37792718del	NC_000009.11:g.37792718del	NC_000009.11:g.37792718dup	NC_000009.11:g.37792717_37792718dup	NC_000009.11:g.37792716_37792718dup	NC_000009.11:g.37792709_37792718dup	NC_000009.11:g.37792718_37792719insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

44 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80804041	Oct 12, 2018 (152)
2	HGSV	ss80824513	Oct 12, 2018 (152)
3	BILGI_BIOE	ss666467659	Apr 25, 2013 (138)
4	SSIP	ss947238310	Aug 21, 2014 (142)
5	1000GENOMES	ss1368229273	Aug 21, 2014 (142)
6	EVA_GENOME_DK	ss1577370867	Apr 01, 2015 (144)
7	HAMMER_LAB	ss1805977525	Sep 08, 2015 (146)
8	SWEGEN	ss3004734854	Nov 08, 2017 (151)
9	MCHAISSO	ss3065225094	Nov 08, 2017 (151)
10	MCHAISSO	ss3066247011	Nov 08, 2017 (151)
11	URBANLAB	ss3649120904	Oct 12, 2018 (152)
12	EVA_DECODE	ss3723898396	Jul 13, 2019 (153)
13	EVA_DECODE	ss3723898397	Jul 13, 2019 (153)
14	EVA_DECODE	ss3723898398	Jul 13, 2019 (153)
15	PACBIO	ss3786405840	Jul 13, 2019 (153)
16	PACBIO	ss3791623825	Jul 13, 2019 (153)
17	PACBIO	ss3796505547	Jul 13, 2019 (153)
18	KHV_HUMAN_GENOMES	ss3812341174	Jul 13, 2019 (153)
19	EVA	ss3831650909	Apr 26, 2020 (154)
20	KRGDB	ss3919668399	Apr 26, 2020 (154)
21	KOGIC	ss3965712192	Apr 26, 2020 (154)
22	KOGIC	ss3965712193	Apr 26, 2020 (154)
23	GNOMAD	ss4201317481	Apr 26, 2021 (155)
24	GNOMAD	ss4201317482	Apr 26, 2021 (155)
25	GNOMAD	ss4201317483	Apr 26, 2021 (155)
26	GNOMAD	ss4201317484	Apr 26, 2021 (155)
27	GNOMAD	ss4201317486	Apr 26, 2021 (155)
28	GNOMAD	ss4201317487	Apr 26, 2021 (155)
29	GNOMAD	ss4201317488	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5193058494	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5193058495	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5193058496	Apr 26, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5280554518	Oct 13, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5280554519	Oct 13, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5280554520	Oct 13, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5280554521	Oct 13, 2022 (156)
37	HUGCELL_USP	ss5476753264	Oct 13, 2022 (156)
38	HUGCELL_USP	ss5476753265	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5476753266	Oct 13, 2022 (156)
40	HUGCELL_USP	ss5476753267	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5736387264	Oct 13, 2022 (156)
42	TOMMO_GENOMICS	ss5736387265	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5736387266	Oct 13, 2022 (156)
44	EVA	ss5829144927	Oct 13, 2022 (156)
45	1000Genomes	NC_000009.11 - 37792702	Oct 12, 2018 (152)
46	The Danish reference pan genome	NC_000009.11 - 37792702	Apr 26, 2020 (154)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 324460187 (NC_000009.12:37792704::T 63503/127556) Row 324460188 (NC_000009.12:37792704::TT 411/127578) Row 324460189 (NC_000009.12:37792704::TTT 1/127596)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 324460187 (NC_000009.12:37792704::T 63503/127556) Row 324460188 (NC_000009.12:37792704::TT 411/127578) Row 324460189 (NC_000009.12:37792704::TTT 1/127596)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 324460187 (NC_000009.12:37792704::T 63503/127556) Row 324460188 (NC_000009.12:37792704::TT 411/127578) Row 324460189 (NC_000009.12:37792704::TTT 1/127596)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 324460187 (NC_000009.12:37792704::T 63503/127556) Row 324460188 (NC_000009.12:37792704::TT 411/127578) Row 324460189 (NC_000009.12:37792704::TTT 1/127596)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 324460187 (NC_000009.12:37792704::T 63503/127556) Row 324460188 (NC_000009.12:37792704::TT 411/127578) Row 324460189 (NC_000009.12:37792704::TTT 1/127596)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 324460187 (NC_000009.12:37792704::T 63503/127556) Row 324460188 (NC_000009.12:37792704::TT 411/127578) Row 324460189 (NC_000009.12:37792704::TTT 1/127596)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 324460187 (NC_000009.12:37792704::T 63503/127556) Row 324460188 (NC_000009.12:37792704::TT 411/127578) Row 324460189 (NC_000009.12:37792704::TTT 1/127596)...	-	Apr 26, 2021 (155)
54	KOREAN population from KRGDB	NC_000009.11 - 37792702	Apr 26, 2020 (154)
55	Korean Genome Project Submission ignored due to conflicting rows: Row 22090193 (NC_000009.12:37792704:T: 188/1832) Row 22090194 (NC_000009.12:37792705::T 437/1832)	-	Apr 26, 2020 (154)
56	Korean Genome Project Submission ignored due to conflicting rows: Row 22090193 (NC_000009.12:37792704:T: 188/1832) Row 22090194 (NC_000009.12:37792705::T 437/1832)	-	Apr 26, 2020 (154)
57	8.3KJPN Submission ignored due to conflicting rows: Row 51027801 (NC_000009.11:37792701::T 3621/16758) Row 51027802 (NC_000009.11:37792701:T: 76/16758) Row 51027803 (NC_000009.11:37792701::TT 14/16758)	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 51027801 (NC_000009.11:37792701::T 3621/16758) Row 51027802 (NC_000009.11:37792701:T: 76/16758) Row 51027803 (NC_000009.11:37792701::TT 14/16758)	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 51027801 (NC_000009.11:37792701::T 3621/16758) Row 51027802 (NC_000009.11:37792701:T: 76/16758) Row 51027803 (NC_000009.11:37792701::TT 14/16758)	-	Apr 26, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 70224368 (NC_000009.12:37792704::T 6274/28258) Row 70224369 (NC_000009.12:37792704:T: 86/28258) Row 70224370 (NC_000009.12:37792704::TT 25/28258)	-	Oct 13, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 70224368 (NC_000009.12:37792704::T 6274/28258) Row 70224369 (NC_000009.12:37792704:T: 86/28258) Row 70224370 (NC_000009.12:37792704::TT 25/28258)	-	Oct 13, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 70224368 (NC_000009.12:37792704::T 6274/28258) Row 70224369 (NC_000009.12:37792704:T: 86/28258) Row 70224370 (NC_000009.12:37792704::TT 25/28258)	-	Oct 13, 2022 (156)
63	ALFA	NC_000009.12 - 37792705	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
ss4201317488	NC_000009.12:37792704:TTT:	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4201317487, ss5280554521, ss5476753267	NC_000009.12:37792704:TT:	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12999788780	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3004734854, ss5193058495	NC_000009.11:37792701:T:	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3649120904, ss3723898396, ss3965712192, ss4201317486, ss5280554520, ss5476753266, ss5736387265	NC_000009.12:37792704:T:	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
12999788780	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
46037071, 1274894, 26845793, ss666467659, ss1368229273, ss1577370867, ss1805977525, ss3786405840, ss3791623825, ss3796505547, ss3831650909, ss3919668399, ss5193058494, ss5829144927	NC_000009.11:37792701::T	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss947238310	NC_000009.11:37792702::T	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3065225094, ss3066247011, ss3812341174, ss4201317481, ss5280554518, ss5476753264, ss5736387264	NC_000009.12:37792704::T	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
12999788780	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3723898397, ss3965712193	NC_000009.12:37792705::T	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss80804041, ss80824513	NT_008413.18:37782718::T	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5193058496	NC_000009.11:37792701::TT	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4201317482, ss5280554519, ss5476753265, ss5736387266	NC_000009.12:37792704::TT	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
12999788780	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3723898398	NC_000009.12:37792705::TT	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4201317483	NC_000009.12:37792704::TTT	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
12999788780	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4201317484	NC_000009.12:37792704::TTTTTTTTTT	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
12999788780	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:37792704:TTTTTTTTTTTT… NC_000009.12:37792704:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs371884745

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

rs371884745