Name: rs36082177
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.

rs36082177

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:15648835-15648852 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₉ / dup(A)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.0000 (0/3028, ALFA)
delA=0.0000 (0/3028, ALFA)
dupA=0.0000 (0/3028, ALFA) (+ 4 more)
dupAA=0.0000 (0/3028, ALFA)
dupAAA=0.0000 (0/3028, ALFA)
dup(A)₄=0.0000 (0/3028, ALFA)
dup(A)₅=0.0000 (0/3028, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DDI2 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	3028	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2070	AAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	524	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	22	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	502	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	8	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
East Asian	Sub	4	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	40	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	220	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	36	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	130	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	3028	(A)₁₈=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	2070	(A)₁₈=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	African	Sub	524	(A)₁₈=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	220	(A)₁₈=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	130	(A)₁₈=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	40	(A)₁₈=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	36	(A)₁₈=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Asian	Sub	8	(A)₁₈=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 1	NC_000001.11:g.15648850_15648852del
GRCh38.p14 chr 1	NC_000001.11:g.15648851_15648852del
GRCh38.p14 chr 1	NC_000001.11:g.15648852del
GRCh38.p14 chr 1	NC_000001.11:g.15648852dup
GRCh38.p14 chr 1	NC_000001.11:g.15648851_15648852dup
GRCh38.p14 chr 1	NC_000001.11:g.15648850_15648852dup
GRCh38.p14 chr 1	NC_000001.11:g.15648849_15648852dup
GRCh38.p14 chr 1	NC_000001.11:g.15648848_15648852dup
GRCh38.p14 chr 1	NC_000001.11:g.15648847_15648852dup
GRCh38.p14 chr 1	NC_000001.11:g.15648846_15648852dup
GRCh38.p14 chr 1	NC_000001.11:g.15648844_15648852dup
GRCh38.p14 chr 1	NC_000001.11:g.15648843_15648852dup
GRCh37.p13 chr 1	NC_000001.10:g.15975345_15975347del
GRCh37.p13 chr 1	NC_000001.10:g.15975346_15975347del
GRCh37.p13 chr 1	NC_000001.10:g.15975347del
GRCh37.p13 chr 1	NC_000001.10:g.15975347dup
GRCh37.p13 chr 1	NC_000001.10:g.15975346_15975347dup
GRCh37.p13 chr 1	NC_000001.10:g.15975345_15975347dup
GRCh37.p13 chr 1	NC_000001.10:g.15975344_15975347dup
GRCh37.p13 chr 1	NC_000001.10:g.15975343_15975347dup
GRCh37.p13 chr 1	NC_000001.10:g.15975342_15975347dup
GRCh37.p13 chr 1	NC_000001.10:g.15975341_15975347dup
GRCh37.p13 chr 1	NC_000001.10:g.15975339_15975347dup
GRCh37.p13 chr 1	NC_000001.10:g.15975338_15975347dup

Gene: DDI2, DNA damage inducible 1 homolog 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DDI2 transcript	NM_032341.5:c.890-870_890… NM_032341.5:c.890-870_890-868del	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(A)₁₈=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₉	dup(A)₁₀
GRCh38.p14 chr 1	NC_000001.11:g.15648835_15648852=	NC_000001.11:g.15648850_15648852del	NC_000001.11:g.15648851_15648852del	NC_000001.11:g.15648852del	NC_000001.11:g.15648852dup	NC_000001.11:g.15648851_15648852dup	NC_000001.11:g.15648850_15648852dup	NC_000001.11:g.15648849_15648852dup	NC_000001.11:g.15648848_15648852dup	NC_000001.11:g.15648847_15648852dup	NC_000001.11:g.15648846_15648852dup	NC_000001.11:g.15648844_15648852dup	NC_000001.11:g.15648843_15648852dup
GRCh37.p13 chr 1	NC_000001.10:g.15975330_15975347=	NC_000001.10:g.15975345_15975347del	NC_000001.10:g.15975346_15975347del	NC_000001.10:g.15975347del	NC_000001.10:g.15975347dup	NC_000001.10:g.15975346_15975347dup	NC_000001.10:g.15975345_15975347dup	NC_000001.10:g.15975344_15975347dup	NC_000001.10:g.15975343_15975347dup	NC_000001.10:g.15975342_15975347dup	NC_000001.10:g.15975341_15975347dup	NC_000001.10:g.15975339_15975347dup	NC_000001.10:g.15975338_15975347dup
DDI2 transcript	NM_032341.4:c.890-885=	NM_032341.4:c.890-870_890-868del	NM_032341.4:c.890-869_890-868del	NM_032341.4:c.890-868del	NM_032341.4:c.890-868dup	NM_032341.4:c.890-869_890-868dup	NM_032341.4:c.890-870_890-868dup	NM_032341.4:c.890-871_890-868dup	NM_032341.4:c.890-872_890-868dup	NM_032341.4:c.890-873_890-868dup	NM_032341.4:c.890-874_890-868dup	NM_032341.4:c.890-876_890-868dup	NM_032341.4:c.890-877_890-868dup
DDI2 transcript	NM_032341.5:c.890-885=	NM_032341.5:c.890-870_890-868del	NM_032341.5:c.890-869_890-868del	NM_032341.5:c.890-868del	NM_032341.5:c.890-868dup	NM_032341.5:c.890-869_890-868dup	NM_032341.5:c.890-870_890-868dup	NM_032341.5:c.890-871_890-868dup	NM_032341.5:c.890-872_890-868dup	NM_032341.5:c.890-873_890-868dup	NM_032341.5:c.890-874_890-868dup	NM_032341.5:c.890-876_890-868dup	NM_032341.5:c.890-877_890-868dup
DDI2 transcript variant X1	XM_005246017.1:c.890-885=	XM_005246017.1:c.890-870_890-868del	XM_005246017.1:c.890-869_890-868del	XM_005246017.1:c.890-868del	XM_005246017.1:c.890-868dup	XM_005246017.1:c.890-869_890-868dup	XM_005246017.1:c.890-870_890-868dup	XM_005246017.1:c.890-871_890-868dup	XM_005246017.1:c.890-872_890-868dup	XM_005246017.1:c.890-873_890-868dup	XM_005246017.1:c.890-874_890-868dup	XM_005246017.1:c.890-876_890-868dup	XM_005246017.1:c.890-877_890-868dup
DDI2 transcript variant X3	XM_005246019.1:c.890-885=	XM_005246019.1:c.890-870_890-868del	XM_005246019.1:c.890-869_890-868del	XM_005246019.1:c.890-868del	XM_005246019.1:c.890-868dup	XM_005246019.1:c.890-869_890-868dup	XM_005246019.1:c.890-870_890-868dup	XM_005246019.1:c.890-871_890-868dup	XM_005246019.1:c.890-872_890-868dup	XM_005246019.1:c.890-873_890-868dup	XM_005246019.1:c.890-874_890-868dup	XM_005246019.1:c.890-876_890-868dup	XM_005246019.1:c.890-877_890-868dup

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#.

51 SubSNP, 27 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41226598	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95222014	Dec 05, 2013 (138)
3	PJP	ss294567062	May 09, 2011 (134)
4	EVA_UK10K_TWINSUK	ss1700298254	Apr 01, 2015 (144)
5	EVA_UK10K_ALSPAC	ss1700298255	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1709909408	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1709909410	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1709912561	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1709912562	Apr 01, 2015 (144)
10	URBANLAB	ss3646607627	Oct 11, 2018 (152)
11	EVA_DECODE	ss3686229046	Jul 12, 2019 (153)
12	EVA_DECODE	ss3686229047	Jul 12, 2019 (153)
13	EVA_DECODE	ss3686229048	Jul 12, 2019 (153)
14	EVA_DECODE	ss3686229049	Jul 12, 2019 (153)
15	EVA_DECODE	ss3686229050	Jul 12, 2019 (153)
16	EVA_DECODE	ss3686229051	Jul 12, 2019 (153)
17	EVA	ss3826039751	Apr 25, 2020 (154)
18	GNOMAD	ss3988885388	Apr 25, 2021 (155)
19	GNOMAD	ss3988885389	Apr 25, 2021 (155)
20	GNOMAD	ss3988885390	Apr 25, 2021 (155)
21	GNOMAD	ss3988885391	Apr 25, 2021 (155)
22	GNOMAD	ss3988885392	Apr 25, 2021 (155)
23	GNOMAD	ss3988885393	Apr 25, 2021 (155)
24	GNOMAD	ss3988885394	Apr 25, 2021 (155)
25	GNOMAD	ss3988885395	Apr 25, 2021 (155)
26	GNOMAD	ss3988885396	Apr 25, 2021 (155)
27	GNOMAD	ss3988885397	Apr 25, 2021 (155)
28	GNOMAD	ss3988885398	Apr 25, 2021 (155)
29	GNOMAD	ss3988885399	Apr 25, 2021 (155)
30	TOMMO_GENOMICS	ss5142639644	Apr 25, 2021 (155)
31	TOMMO_GENOMICS	ss5142639645	Apr 25, 2021 (155)
32	TOMMO_GENOMICS	ss5142639646	Apr 25, 2021 (155)
33	TOMMO_GENOMICS	ss5142639647	Apr 25, 2021 (155)
34	TOMMO_GENOMICS	ss5142639648	Apr 25, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5241301626	Oct 12, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5241301627	Oct 12, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5241301628	Oct 12, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5241301629	Oct 12, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5241301630	Oct 12, 2022 (156)
40	HUGCELL_USP	ss5442481565	Oct 12, 2022 (156)
41	HUGCELL_USP	ss5442481566	Oct 12, 2022 (156)
42	HUGCELL_USP	ss5442481567	Oct 12, 2022 (156)
43	HUGCELL_USP	ss5442481568	Oct 12, 2022 (156)
44	HUGCELL_USP	ss5442481569	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5666997456	Oct 12, 2022 (156)
46	TOMMO_GENOMICS	ss5666997457	Oct 12, 2022 (156)
47	TOMMO_GENOMICS	ss5666997459	Oct 12, 2022 (156)
48	TOMMO_GENOMICS	ss5666997460	Oct 12, 2022 (156)
49	EVA	ss5831584860	Oct 12, 2022 (156)
50	EVA	ss5831584861	Oct 12, 2022 (156)
51	EVA	ss5831584862	Oct 12, 2022 (156)
52	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 256843 (NC_000001.10:15975329:AA: 423/3854) Row 256844 (NC_000001.10:15975329::AA 1011/3854)	-	Oct 11, 2018 (152)
53	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 256843 (NC_000001.10:15975329:AA: 423/3854) Row 256844 (NC_000001.10:15975329::AA 1011/3854)	-	Oct 11, 2018 (152)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3416340 (NC_000001.11:15648834::A 3565/88418) Row 3416341 (NC_000001.11:15648834::AA 24939/87600) Row 3416342 (NC_000001.11:15648834::AAA 1348/87618)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3416340 (NC_000001.11:15648834::A 3565/88418) Row 3416341 (NC_000001.11:15648834::AA 24939/87600) Row 3416342 (NC_000001.11:15648834::AAA 1348/87618)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3416340 (NC_000001.11:15648834::A 3565/88418) Row 3416341 (NC_000001.11:15648834::AA 24939/87600) Row 3416342 (NC_000001.11:15648834::AAA 1348/87618)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3416340 (NC_000001.11:15648834::A 3565/88418) Row 3416341 (NC_000001.11:15648834::AA 24939/87600) Row 3416342 (NC_000001.11:15648834::AAA 1348/87618)...	-	Apr 25, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3416340 (NC_000001.11:15648834::A 3565/88418) Row 3416341 (NC_000001.11:15648834::AA 24939/87600) Row 3416342 (NC_000001.11:15648834::AAA 1348/87618)...	-	Apr 25, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3416340 (NC_000001.11:15648834::A 3565/88418) Row 3416341 (NC_000001.11:15648834::AA 24939/87600) Row 3416342 (NC_000001.11:15648834::AAA 1348/87618)...	-	Apr 25, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3416340 (NC_000001.11:15648834::A 3565/88418) Row 3416341 (NC_000001.11:15648834::AA 24939/87600) Row 3416342 (NC_000001.11:15648834::AAA 1348/87618)...	-	Apr 25, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3416340 (NC_000001.11:15648834::A 3565/88418) Row 3416341 (NC_000001.11:15648834::AA 24939/87600) Row 3416342 (NC_000001.11:15648834::AAA 1348/87618)...	-	Apr 25, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3416340 (NC_000001.11:15648834::A 3565/88418) Row 3416341 (NC_000001.11:15648834::AA 24939/87600) Row 3416342 (NC_000001.11:15648834::AAA 1348/87618)...	-	Apr 25, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3416340 (NC_000001.11:15648834::A 3565/88418) Row 3416341 (NC_000001.11:15648834::AA 24939/87600) Row 3416342 (NC_000001.11:15648834::AAA 1348/87618)...	-	Apr 25, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3416340 (NC_000001.11:15648834::A 3565/88418) Row 3416341 (NC_000001.11:15648834::AA 24939/87600) Row 3416342 (NC_000001.11:15648834::AAA 1348/87618)...	-	Apr 25, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 3416340 (NC_000001.11:15648834::A 3565/88418) Row 3416341 (NC_000001.11:15648834::AA 24939/87600) Row 3416342 (NC_000001.11:15648834::AAA 1348/87618)...	-	Apr 25, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 608951 (NC_000001.10:15975329:A: 8148/16666) Row 608952 (NC_000001.10:15975329::AA 899/16666) Row 608953 (NC_000001.10:15975329::A 211/16666)...	-	Apr 25, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 608951 (NC_000001.10:15975329:A: 8148/16666) Row 608952 (NC_000001.10:15975329::AA 899/16666) Row 608953 (NC_000001.10:15975329::A 211/16666)...	-	Apr 25, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 608951 (NC_000001.10:15975329:A: 8148/16666) Row 608952 (NC_000001.10:15975329::AA 899/16666) Row 608953 (NC_000001.10:15975329::A 211/16666)...	-	Apr 25, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 608951 (NC_000001.10:15975329:A: 8148/16666) Row 608952 (NC_000001.10:15975329::AA 899/16666) Row 608953 (NC_000001.10:15975329::A 211/16666)...	-	Apr 25, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 608951 (NC_000001.10:15975329:A: 8148/16666) Row 608952 (NC_000001.10:15975329::AA 899/16666) Row 608953 (NC_000001.10:15975329::A 211/16666)...	-	Apr 25, 2021 (155)
71	14KJPN Submission ignored due to conflicting rows: Row 834560 (NC_000001.11:15648834:A: 14259/28242) Row 834561 (NC_000001.11:15648834::AA 1440/28242) Row 834563 (NC_000001.11:15648834::A 383/28242)...	-	Oct 12, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 834560 (NC_000001.11:15648834:A: 14259/28242) Row 834561 (NC_000001.11:15648834::AA 1440/28242) Row 834563 (NC_000001.11:15648834::A 383/28242)...	-	Oct 12, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 834560 (NC_000001.11:15648834:A: 14259/28242) Row 834561 (NC_000001.11:15648834::AA 1440/28242) Row 834563 (NC_000001.11:15648834::A 383/28242)...	-	Oct 12, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 834560 (NC_000001.11:15648834:A: 14259/28242) Row 834561 (NC_000001.11:15648834::AA 1440/28242) Row 834563 (NC_000001.11:15648834::A 383/28242)...	-	Oct 12, 2022 (156)
75	UK 10K study - Twins Submission ignored due to conflicting rows: Row 256843 (NC_000001.10:15975329:AA: 413/3708) Row 256844 (NC_000001.10:15975329::AA 939/3708)	-	Oct 11, 2018 (152)
76	UK 10K study - Twins Submission ignored due to conflicting rows: Row 256843 (NC_000001.10:15975329:AA: 413/3708) Row 256844 (NC_000001.10:15975329::AA 939/3708)	-	Oct 11, 2018 (152)
77	UK 10K study - Twins Submission ignored due to conflicting rows: Row 256843 (NC_000001.10:15975329:AA: 413/3708) Row 256844 (NC_000001.10:15975331::AA 939/3708) Row 256845 (NC_000001.10:15975330:A: 1242/3708)	-	Apr 25, 2020 (154)
78	ALFA	NC_000001.11 - 15648835	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).

Associated ID	History Updated (Build)
rs71002916	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3988885399	NC_000001.11:15648834:AAA:	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss1700298254, ss1700298255, ss5142639647, ss5831584861	NC_000001.10:15975329:AA:	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3686229051, ss3988885398, ss5442481565	NC_000001.11:15648834:AA:	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
1954549479	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss294567062	NC_000001.9:15847916:A:	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5142639644, ss5831584862	NC_000001.10:15975329:A:	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss1709909410, ss1709912562	NC_000001.10:15975330:A:	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3646607627, ss3988885397, ss5241301629, ss5442481566, ss5666997456	NC_000001.11:15648834:A:	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
1954549479	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3686229050	NC_000001.11:15648835:A:	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss41226598	NT_004610.19:2655417:A:	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss95222014	NT_004610.19:2655434:A:	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5142639646	NC_000001.10:15975329::A	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3988885388, ss5241301630, ss5442481567, ss5666997459	NC_000001.11:15648834::A	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
1954549479	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3686229049	NC_000001.11:15648836::A	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3826039751, ss5142639645, ss5831584860	NC_000001.10:15975329::AA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss1709909408, ss1709912561	NC_000001.10:15975331::AA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3988885389, ss5241301626, ss5442481568, ss5666997457	NC_000001.11:15648834::AA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
1954549479	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3686229048	NC_000001.11:15648836::AA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5142639648	NC_000001.10:15975329::AAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3988885390, ss5241301627, ss5442481569, ss5666997460	NC_000001.11:15648834::AAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
1954549479	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3686229047	NC_000001.11:15648836::AAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3988885391, ss5241301628	NC_000001.11:15648834::AAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
1954549479	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3686229046	NC_000001.11:15648836::AAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3988885392	NC_000001.11:15648834::AAAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
1954549479	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3988885393	NC_000001.11:15648834::AAAAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3988885394	NC_000001.11:15648834::AAAAAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3988885395	NC_000001.11:15648834::AAAAAAAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3988885396	NC_000001.11:15648834::AAAAAAAAAA	NC_000001.11:15648834:AAAAAAAAAAAA… NC_000001.11:15648834:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs36082177

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

rs36082177