Name: rs71586738
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.

rs71586738

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:92216319-92216331 (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)₈ / del(T)₇ / del(T)₆ / del(…
del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₈=0.00000 (0/10322, ALFA)
del(T)₇=0.00000 (0/10322, ALFA)
del(T)₆=0.00000 (0/10322, ALFA) (+ 11 more)
del(T)₅=0.00000 (0/10322, ALFA)
del(T)₄=0.00000 (0/10322, ALFA)
delTTT=0.00000 (0/10322, ALFA)
delTT=0.00000 (0/10322, ALFA)
delT=0.00000 (0/10322, ALFA)
dupT=0.00000 (0/10322, ALFA)
dupTT=0.00000 (0/10322, ALFA)
dupTTT=0.00000 (0/10322, ALFA)
dup(T)₄=0.00000 (0/10322, ALFA)
dup(T)₅=0.00000 (0/10322, ALFA)
dup(T)₇=0.00000 (0/10322, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: C1orf146 : 2KB Upstream 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	10322	TTTTTTTTTTTTT=1.00000	TTTTT=0.00000, TTTTTT=0.00000, TTTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	6308	TTTTTTTTTTTTT=1.0000	TTTTT=0.0000, TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2702	TTTTTTTTTTTTT=1.0000	TTTTT=0.0000, TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	104	TTTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
African American	Sub	2598	TTTTTTTTTTTTT=1.0000	TTTTT=0.0000, TTTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	100	TTTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	80	TTTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	20	TTTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	140	TTTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	550	TTTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	90	TTTTTTTTTTTTT=1.00	TTTTT=0.00, TTTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	432	TTTTTTTTTTTTT=1.000	TTTTT=0.000, TTTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	10322	(T)₁₃=1.00000	del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₇=0.00000
Allele Frequency Aggregator	European	Sub	6308	(T)₁₃=1.0000	del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	African	Sub	2702	(T)₁₃=1.0000	del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	550	(T)₁₃=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	432	(T)₁₃=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	140	(T)₁₃=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Asian	Sub	100	(T)₁₃=1.00	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	90	(T)₁₃=1.00	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₇=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 1	NC_000001.11:g.92216324_92216331del
GRCh38.p14 chr 1	NC_000001.11:g.92216325_92216331del
GRCh38.p14 chr 1	NC_000001.11:g.92216326_92216331del
GRCh38.p14 chr 1	NC_000001.11:g.92216327_92216331del
GRCh38.p14 chr 1	NC_000001.11:g.92216328_92216331del
GRCh38.p14 chr 1	NC_000001.11:g.92216329_92216331del
GRCh38.p14 chr 1	NC_000001.11:g.92216330_92216331del
GRCh38.p14 chr 1	NC_000001.11:g.92216331del
GRCh38.p14 chr 1	NC_000001.11:g.92216331dup
GRCh38.p14 chr 1	NC_000001.11:g.92216330_92216331dup
GRCh38.p14 chr 1	NC_000001.11:g.92216329_92216331dup
GRCh38.p14 chr 1	NC_000001.11:g.92216328_92216331dup
GRCh38.p14 chr 1	NC_000001.11:g.92216327_92216331dup
GRCh38.p14 chr 1	NC_000001.11:g.92216326_92216331dup
GRCh38.p14 chr 1	NC_000001.11:g.92216325_92216331dup
GRCh37.p13 chr 1	NC_000001.10:g.92681881_92681888del
GRCh37.p13 chr 1	NC_000001.10:g.92681882_92681888del
GRCh37.p13 chr 1	NC_000001.10:g.92681883_92681888del
GRCh37.p13 chr 1	NC_000001.10:g.92681884_92681888del
GRCh37.p13 chr 1	NC_000001.10:g.92681885_92681888del
GRCh37.p13 chr 1	NC_000001.10:g.92681886_92681888del
GRCh37.p13 chr 1	NC_000001.10:g.92681887_92681888del
GRCh37.p13 chr 1	NC_000001.10:g.92681888del
GRCh37.p13 chr 1	NC_000001.10:g.92681888dup
GRCh37.p13 chr 1	NC_000001.10:g.92681887_92681888dup
GRCh37.p13 chr 1	NC_000001.10:g.92681886_92681888dup
GRCh37.p13 chr 1	NC_000001.10:g.92681885_92681888dup
GRCh37.p13 chr 1	NC_000001.10:g.92681884_92681888dup
GRCh37.p13 chr 1	NC_000001.10:g.92681883_92681888dup
GRCh37.p13 chr 1	NC_000001.10:g.92681882_92681888dup

Gene: C1orf146, chromosome 1 open reading frame 146 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
C1orf146 transcript	NM_001012425.2:c.	N/A	Upstream Transcript Variant
C1orf146 transcript variant X1	XM_011541447.3:c.	N/A	Upstream Transcript Variant
C1orf146 transcript variant X3	XM_047420086.1:c.	N/A	Upstream Transcript Variant
C1orf146 transcript variant X2	XM_047420085.1:c.	N/A	N/A

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)₁₃=	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇
GRCh38.p14 chr 1	NC_000001.11:g.92216319_92216331=	NC_000001.11:g.92216324_92216331del	NC_000001.11:g.92216325_92216331del	NC_000001.11:g.92216326_92216331del	NC_000001.11:g.92216327_92216331del	NC_000001.11:g.92216328_92216331del	NC_000001.11:g.92216329_92216331del	NC_000001.11:g.92216330_92216331del	NC_000001.11:g.92216331del	NC_000001.11:g.92216331dup	NC_000001.11:g.92216330_92216331dup	NC_000001.11:g.92216329_92216331dup	NC_000001.11:g.92216328_92216331dup	NC_000001.11:g.92216327_92216331dup	NC_000001.11:g.92216326_92216331dup	NC_000001.11:g.92216325_92216331dup
GRCh37.p13 chr 1	NC_000001.10:g.92681876_92681888=	NC_000001.10:g.92681881_92681888del	NC_000001.10:g.92681882_92681888del	NC_000001.10:g.92681883_92681888del	NC_000001.10:g.92681884_92681888del	NC_000001.10:g.92681885_92681888del	NC_000001.10:g.92681886_92681888del	NC_000001.10:g.92681887_92681888del	NC_000001.10:g.92681888del	NC_000001.10:g.92681888dup	NC_000001.10:g.92681887_92681888dup	NC_000001.10:g.92681886_92681888dup	NC_000001.10:g.92681885_92681888dup	NC_000001.10:g.92681884_92681888dup	NC_000001.10:g.92681883_92681888dup	NC_000001.10:g.92681882_92681888dup

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#.

27 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss98573431	Feb 13, 2009 (130)
2	EVA_DECODE	ss3687270190	Jul 12, 2019 (153)
3	EVA_DECODE	ss3687270191	Jul 12, 2019 (153)
4	EVA_DECODE	ss3687270192	Jul 12, 2019 (153)
5	EVA_DECODE	ss3687270193	Jul 12, 2019 (153)
6	GNOMAD	ss3998105024	Apr 25, 2021 (155)
7	GNOMAD	ss3998105040	Apr 25, 2021 (155)
8	GNOMAD	ss3998105041	Apr 25, 2021 (155)
9	GNOMAD	ss3998105042	Apr 25, 2021 (155)
10	GNOMAD	ss3998105043	Apr 25, 2021 (155)
11	GNOMAD	ss3998105044	Apr 25, 2021 (155)
12	GNOMAD	ss3998105045	Apr 25, 2021 (155)
13	GNOMAD	ss3998105046	Apr 25, 2021 (155)
14	GNOMAD	ss3998105047	Apr 25, 2021 (155)
15	GNOMAD	ss3998105048	Apr 25, 2021 (155)
16	GNOMAD	ss3998105049	Apr 25, 2021 (155)
17	GNOMAD	ss3998105050	Apr 25, 2021 (155)
18	TOMMO_GENOMICS	ss5145088155	Apr 25, 2021 (155)
19	TOMMO_GENOMICS	ss5145088156	Apr 25, 2021 (155)
20	TOMMO_GENOMICS	ss5145088157	Apr 25, 2021 (155)
21	1000G_HIGH_COVERAGE	ss5243152337	Oct 12, 2022 (156)
22	1000G_HIGH_COVERAGE	ss5243152338	Oct 12, 2022 (156)
23	1000G_HIGH_COVERAGE	ss5243152339	Oct 12, 2022 (156)
24	HUGCELL_USP	ss5444120962	Oct 12, 2022 (156)
25	HUGCELL_USP	ss5444120964	Oct 12, 2022 (156)
26	TOMMO_GENOMICS	ss5670183189	Oct 12, 2022 (156)
27	TOMMO_GENOMICS	ss5670183190	Oct 12, 2022 (156)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18818388 (NC_000001.11:92216318::T 2557/93792) Row 18818404 (NC_000001.11:92216318::TT 31/93904) Row 18818405 (NC_000001.11:92216318::TTT 29/93892)...	-	Apr 25, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18818388 (NC_000001.11:92216318::T 2557/93792) Row 18818404 (NC_000001.11:92216318::TT 31/93904) Row 18818405 (NC_000001.11:92216318::TTT 29/93892)...	-	Apr 25, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18818388 (NC_000001.11:92216318::T 2557/93792) Row 18818404 (NC_000001.11:92216318::TT 31/93904) Row 18818405 (NC_000001.11:92216318::TTT 29/93892)...	-	Apr 25, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18818388 (NC_000001.11:92216318::T 2557/93792) Row 18818404 (NC_000001.11:92216318::TT 31/93904) Row 18818405 (NC_000001.11:92216318::TTT 29/93892)...	-	Apr 25, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18818388 (NC_000001.11:92216318::T 2557/93792) Row 18818404 (NC_000001.11:92216318::TT 31/93904) Row 18818405 (NC_000001.11:92216318::TTT 29/93892)...	-	Apr 25, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18818388 (NC_000001.11:92216318::T 2557/93792) Row 18818404 (NC_000001.11:92216318::TT 31/93904) Row 18818405 (NC_000001.11:92216318::TTT 29/93892)...	-	Apr 25, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18818388 (NC_000001.11:92216318::T 2557/93792) Row 18818404 (NC_000001.11:92216318::TT 31/93904) Row 18818405 (NC_000001.11:92216318::TTT 29/93892)...	-	Apr 25, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18818388 (NC_000001.11:92216318::T 2557/93792) Row 18818404 (NC_000001.11:92216318::TT 31/93904) Row 18818405 (NC_000001.11:92216318::TTT 29/93892)...	-	Apr 25, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18818388 (NC_000001.11:92216318::T 2557/93792) Row 18818404 (NC_000001.11:92216318::TT 31/93904) Row 18818405 (NC_000001.11:92216318::TTT 29/93892)...	-	Apr 25, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18818388 (NC_000001.11:92216318::T 2557/93792) Row 18818404 (NC_000001.11:92216318::TT 31/93904) Row 18818405 (NC_000001.11:92216318::TTT 29/93892)...	-	Apr 25, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18818388 (NC_000001.11:92216318::T 2557/93792) Row 18818404 (NC_000001.11:92216318::TT 31/93904) Row 18818405 (NC_000001.11:92216318::TTT 29/93892)...	-	Apr 25, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 18818388 (NC_000001.11:92216318::T 2557/93792) Row 18818404 (NC_000001.11:92216318::TT 31/93904) Row 18818405 (NC_000001.11:92216318::TTT 29/93892)...	-	Apr 25, 2021 (155)
40	8.3KJPN Submission ignored due to conflicting rows: Row 3057462 (NC_000001.10:92681875::T 13/16380) Row 3057463 (NC_000001.10:92681875::TTT 1/16380) Row 3057464 (NC_000001.10:92681875:T: 5/16380)	-	Apr 25, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 3057462 (NC_000001.10:92681875::T 13/16380) Row 3057463 (NC_000001.10:92681875::TTT 1/16380) Row 3057464 (NC_000001.10:92681875:T: 5/16380)	-	Apr 25, 2021 (155)
42	8.3KJPN Submission ignored due to conflicting rows: Row 3057462 (NC_000001.10:92681875::T 13/16380) Row 3057463 (NC_000001.10:92681875::TTT 1/16380) Row 3057464 (NC_000001.10:92681875:T: 5/16380)	-	Apr 25, 2021 (155)
43	14KJPN Submission ignored due to conflicting rows: Row 4020293 (NC_000001.11:92216318:T: 7/27984) Row 4020294 (NC_000001.11:92216318::T 22/27984)	-	Oct 12, 2022 (156)
44	14KJPN Submission ignored due to conflicting rows: Row 4020293 (NC_000001.11:92216318:T: 7/27984) Row 4020294 (NC_000001.11:92216318::T 22/27984)	-	Oct 12, 2022 (156)
45	ALFA	NC_000001.11 - 92216319	Apr 25, 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
ss3998105050	NC_000001.11:92216318:TTTTTTTT:	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTT	(self)
ss3998105049	NC_000001.11:92216318:TTTTTT:	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTT	(self)
ss3998105048	NC_000001.11:92216318:TTTTT:	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTT	(self)
ss3998105047	NC_000001.11:92216318:TTTT:	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTT	(self)
ss3998105046	NC_000001.11:92216318:TTT:	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3998105045	NC_000001.11:92216318:TT:	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss5145088157	NC_000001.10:92681875:T:	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3687270190, ss3998105044, ss5243152338, ss5444120962, ss5670183189	NC_000001.11:92216318:T:	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss98573431	NT_032977.9:62653805:T:	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5145088155	NC_000001.10:92681875::T	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3998105024, ss5243152339, ss5444120964, ss5670183190	NC_000001.11:92216318::T	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3998105040	NC_000001.11:92216318::TT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3687270191	NC_000001.11:92216319::TT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5145088156	NC_000001.10:92681875::TTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3998105041, ss5243152337	NC_000001.11:92216318::TTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3687270192	NC_000001.11:92216319::TTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3998105042	NC_000001.11:92216318::TTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3687270193	NC_000001.11:92216319::TTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3998105043	NC_000001.11:92216318::TTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
13496669044	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3083325095	NC_000001.11:92216318::TTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT
ss3083325096	NC_000001.11:92216318::TTTTTTT	NC_000001.11:92216318:TTTTTTTTTTTT… NC_000001.11:92216318:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

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

No publications for rs71586738

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

rs71586738