Name: rs35876784
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.

rs35876784

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:30046080-30046094 (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)₁₃
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.00474 (66/13914, ALFA)
delA=0.025 (15/598, NorthernSweden)
delA=0.07 (3/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HTRZ	HWEP
Total	Global	13914	AAAAAAAAAAAAAAA=0.99454	AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00474, AAAAAAAAAAAAAAAA=0.00072, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000	0.990475	0.009525	0
European	Sub	11658	AAAAAAAAAAAAAAA=0.99357	AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00558, AAAAAAAAAAAAAAAA=0.00086, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000	0.988795	0.011205	0
African	Sub	1052	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	N/A
African Others	Sub	38	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
African American	Sub	1014	AAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	N/A
Asian	Sub	100	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
East Asian	Sub	76	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
Other Asian	Sub	24	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
Latin American 1	Sub	112	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
Latin American 2	Sub	560	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
South Asian	Sub	72	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
Other	Sub	360	AAAAAAAAAAAAAAA=0.997	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.003, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	0.994444	0.005556	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	13914	(A)₁₅=0.99454	delAAA=0.00000, delAA=0.00000, delA=0.00474, dupA=0.00072, dupAA=0.00000, dupAAA=0.00000, dup(A)₄=0.00000
Allele Frequency Aggregator	European	Sub	11658	(A)₁₅=0.99357	delAAA=0.00000, delAA=0.00000, delA=0.00558, dupA=0.00086, dupAA=0.00000, dupAAA=0.00000, dup(A)₄=0.00000
Allele Frequency Aggregator	African	Sub	1052	(A)₁₅=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	560	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	360	(A)₁₅=0.997	delAAA=0.000, delAA=0.000, delA=0.003, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	112	(A)₁₅=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Asian	Sub	100	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	72	(A)₁₅=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Northern Sweden	ACPOP	Study-wide	598	(A)₁₅=0.975	delA=0.025
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₅=0.93	delA=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 15	NC_000015.10:g.30046092_30046094del
GRCh38.p14 chr 15	NC_000015.10:g.30046093_30046094del
GRCh38.p14 chr 15	NC_000015.10:g.30046094del
GRCh38.p14 chr 15	NC_000015.10:g.30046094dup
GRCh38.p14 chr 15	NC_000015.10:g.30046093_30046094dup
GRCh38.p14 chr 15	NC_000015.10:g.30046092_30046094dup
GRCh38.p14 chr 15	NC_000015.10:g.30046091_30046094dup
GRCh38.p14 chr 15	NC_000015.10:g.30046082_30046094dup
GRCh37.p13 chr 15	NC_000015.9:g.30338295_30338297del
GRCh37.p13 chr 15	NC_000015.9:g.30338296_30338297del
GRCh37.p13 chr 15	NC_000015.9:g.30338297del
GRCh37.p13 chr 15	NC_000015.9:g.30338297dup
GRCh37.p13 chr 15	NC_000015.9:g.30338296_30338297dup
GRCh37.p13 chr 15	NC_000015.9:g.30338295_30338297dup
GRCh37.p13 chr 15	NC_000015.9:g.30338294_30338297dup
GRCh37.p13 chr 15	NC_000015.9:g.30338285_30338297dup
SYNGR2P1 pseudogene	NG_003218.3:g.1753_1755del
SYNGR2P1 pseudogene	NG_003218.3:g.1754_1755del
SYNGR2P1 pseudogene	NG_003218.3:g.1755del
SYNGR2P1 pseudogene	NG_003218.3:g.1755dup
SYNGR2P1 pseudogene	NG_003218.3:g.1754_1755dup
SYNGR2P1 pseudogene	NG_003218.3:g.1753_1755dup
SYNGR2P1 pseudogene	NG_003218.3:g.1752_1755dup
SYNGR2P1 pseudogene	NG_003218.3:g.1743_1755dup
GRCh38.p14 chr 15 novel patch HSCHR15_6_CTG8	NW_012132920.1:g.33772_33774del
GRCh38.p14 chr 15 novel patch HSCHR15_6_CTG8	NW_012132920.1:g.33773_33774del
GRCh38.p14 chr 15 novel patch HSCHR15_6_CTG8	NW_012132920.1:g.33774del
GRCh38.p14 chr 15 novel patch HSCHR15_6_CTG8	NW_012132920.1:g.33774dup
GRCh38.p14 chr 15 novel patch HSCHR15_6_CTG8	NW_012132920.1:g.33773_33774dup
GRCh38.p14 chr 15 novel patch HSCHR15_6_CTG8	NW_012132920.1:g.33772_33774dup
GRCh38.p14 chr 15 novel patch HSCHR15_6_CTG8	NW_012132920.1:g.33771_33774dup
GRCh38.p14 chr 15 novel patch HSCHR15_6_CTG8	NW_012132920.1:g.33762_33774dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.2218809_2218811del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.2218810_2218811del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.2218811del
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.2218811dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.2218810_2218811dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.2218809_2218811dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.2218808_2218811dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.2218799_2218811dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.2331293_2331295del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.2331294_2331295del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.2331295del
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.2331295dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.2331294_2331295dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.2331293_2331295dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.2331292_2331295dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.2331283_2331295dup

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)₁₅=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₁₃
GRCh38.p14 chr 15	NC_000015.10:g.30046080_30046094=	NC_000015.10:g.30046092_30046094del	NC_000015.10:g.30046093_30046094del	NC_000015.10:g.30046094del	NC_000015.10:g.30046094dup	NC_000015.10:g.30046093_30046094dup	NC_000015.10:g.30046092_30046094dup	NC_000015.10:g.30046091_30046094dup	NC_000015.10:g.30046082_30046094dup
GRCh37.p13 chr 15	NC_000015.9:g.30338283_30338297=	NC_000015.9:g.30338295_30338297del	NC_000015.9:g.30338296_30338297del	NC_000015.9:g.30338297del	NC_000015.9:g.30338297dup	NC_000015.9:g.30338296_30338297dup	NC_000015.9:g.30338295_30338297dup	NC_000015.9:g.30338294_30338297dup	NC_000015.9:g.30338285_30338297dup
SYNGR2P1 pseudogene	NG_003218.3:g.1741_1755=	NG_003218.3:g.1753_1755del	NG_003218.3:g.1754_1755del	NG_003218.3:g.1755del	NG_003218.3:g.1755dup	NG_003218.3:g.1754_1755dup	NG_003218.3:g.1753_1755dup	NG_003218.3:g.1752_1755dup	NG_003218.3:g.1743_1755dup
GRCh38.p14 chr 15 novel patch HSCHR15_6_CTG8	NW_012132920.1:g.33760_33774=	NW_012132920.1:g.33772_33774del	NW_012132920.1:g.33773_33774del	NW_012132920.1:g.33774del	NW_012132920.1:g.33774dup	NW_012132920.1:g.33773_33774dup	NW_012132920.1:g.33772_33774dup	NW_012132920.1:g.33771_33774dup	NW_012132920.1:g.33762_33774dup
GRCh38.p14 chr 15 fix patch HG2139_PATCH	NW_011332701.1:g.2218797_2218811=	NW_011332701.1:g.2218809_2218811del	NW_011332701.1:g.2218810_2218811del	NW_011332701.1:g.2218811del	NW_011332701.1:g.2218811dup	NW_011332701.1:g.2218810_2218811dup	NW_011332701.1:g.2218809_2218811dup	NW_011332701.1:g.2218808_2218811dup	NW_011332701.1:g.2218799_2218811dup
GRCh38.p14 chr 15 alt locus HSCHR15_4_CTG8	NT_187660.1:g.2331281_2331295=	NT_187660.1:g.2331293_2331295del	NT_187660.1:g.2331294_2331295del	NT_187660.1:g.2331295del	NT_187660.1:g.2331295dup	NT_187660.1:g.2331294_2331295dup	NT_187660.1:g.2331293_2331295dup	NT_187660.1:g.2331292_2331295dup	NT_187660.1:g.2331283_2331295dup

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#.

32 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40538853	Dec 03, 2013 (138)
2	GMI	ss289248839	May 04, 2012 (137)
3	EVA_GENOME_DK	ss1574838455	Apr 01, 2015 (144)
4	SWEGEN	ss3013031173	Nov 08, 2017 (151)
5	ACPOP	ss3740797689	Jul 13, 2019 (153)
6	PACBIO	ss3787804430	Jul 13, 2019 (153)
7	EVA	ss3834162191	Apr 27, 2020 (154)
8	EVA	ss3840677842	Apr 27, 2020 (154)
9	EVA	ss3846166615	Apr 27, 2020 (154)
10	GNOMAD	ss4286155946	Apr 27, 2021 (155)
11	GNOMAD	ss4286155947	Apr 27, 2021 (155)
12	GNOMAD	ss4286155948	Apr 27, 2021 (155)
13	GNOMAD	ss4286155949	Apr 27, 2021 (155)
14	GNOMAD	ss4286155950	Apr 27, 2021 (155)
15	GNOMAD	ss4286155951	Apr 27, 2021 (155)
16	GNOMAD	ss4286155952	Apr 27, 2021 (155)
17	TOMMO_GENOMICS	ss5215478803	Apr 27, 2021 (155)
18	TOMMO_GENOMICS	ss5215478804	Apr 27, 2021 (155)
19	TOMMO_GENOMICS	ss5215478805	Apr 27, 2021 (155)
20	1000G_HIGH_COVERAGE	ss5297911900	Oct 16, 2022 (156)
21	1000G_HIGH_COVERAGE	ss5297911901	Oct 16, 2022 (156)
22	1000G_HIGH_COVERAGE	ss5297911902	Oct 16, 2022 (156)
23	1000G_HIGH_COVERAGE	ss5297911903	Oct 16, 2022 (156)
24	1000G_HIGH_COVERAGE	ss5297911904	Oct 16, 2022 (156)
25	HUGCELL_USP	ss5491713991	Oct 16, 2022 (156)
26	HUGCELL_USP	ss5491713992	Oct 16, 2022 (156)
27	HUGCELL_USP	ss5491713993	Oct 16, 2022 (156)
28	HUGCELL_USP	ss5491713994	Oct 16, 2022 (156)
29	TOMMO_GENOMICS	ss5769074337	Oct 16, 2022 (156)
30	TOMMO_GENOMICS	ss5769074338	Oct 16, 2022 (156)
31	TOMMO_GENOMICS	ss5769074339	Oct 16, 2022 (156)
32	EVA	ss5851232181	Oct 16, 2022 (156)
33	The Danish reference pan genome	NC_000015.9 - 30338283	Apr 27, 2020 (154)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464671527 (NC_000015.10:30046079::A 3040/121460) Row 464671528 (NC_000015.10:30046079::AA 5025/121556) Row 464671529 (NC_000015.10:30046079::AAA 1321/121600)...	-	Apr 27, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464671527 (NC_000015.10:30046079::A 3040/121460) Row 464671528 (NC_000015.10:30046079::AA 5025/121556) Row 464671529 (NC_000015.10:30046079::AAA 1321/121600)...	-	Apr 27, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464671527 (NC_000015.10:30046079::A 3040/121460) Row 464671528 (NC_000015.10:30046079::AA 5025/121556) Row 464671529 (NC_000015.10:30046079::AAA 1321/121600)...	-	Apr 27, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464671527 (NC_000015.10:30046079::A 3040/121460) Row 464671528 (NC_000015.10:30046079::AA 5025/121556) Row 464671529 (NC_000015.10:30046079::AAA 1321/121600)...	-	Apr 27, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464671527 (NC_000015.10:30046079::A 3040/121460) Row 464671528 (NC_000015.10:30046079::AA 5025/121556) Row 464671529 (NC_000015.10:30046079::AAA 1321/121600)...	-	Apr 27, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464671527 (NC_000015.10:30046079::A 3040/121460) Row 464671528 (NC_000015.10:30046079::AA 5025/121556) Row 464671529 (NC_000015.10:30046079::AAA 1321/121600)...	-	Apr 27, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 464671527 (NC_000015.10:30046079::A 3040/121460) Row 464671528 (NC_000015.10:30046079::AA 5025/121556) Row 464671529 (NC_000015.10:30046079::AAA 1321/121600)...	-	Apr 27, 2021 (155)
41	Northern Sweden	NC_000015.9 - 30338283	Jul 13, 2019 (153)
42	8.3KJPN Submission ignored due to conflicting rows: Row 73448110 (NC_000015.9:30338282::A 48/16760) Row 73448111 (NC_000015.9:30338282:A: 916/16760) Row 73448112 (NC_000015.9:30338282:AA: 1/16760)	-	Apr 27, 2021 (155)
43	8.3KJPN Submission ignored due to conflicting rows: Row 73448110 (NC_000015.9:30338282::A 48/16760) Row 73448111 (NC_000015.9:30338282:A: 916/16760) Row 73448112 (NC_000015.9:30338282:AA: 1/16760)	-	Apr 27, 2021 (155)
44	8.3KJPN Submission ignored due to conflicting rows: Row 73448110 (NC_000015.9:30338282::A 48/16760) Row 73448111 (NC_000015.9:30338282:A: 916/16760) Row 73448112 (NC_000015.9:30338282:AA: 1/16760)	-	Apr 27, 2021 (155)
45	14KJPN Submission ignored due to conflicting rows: Row 102911441 (NC_000015.10:30046079:A: 1532/28258) Row 102911442 (NC_000015.10:30046079::A 78/28258) Row 102911443 (NC_000015.10:30046079:AA: 2/28258)	-	Oct 16, 2022 (156)
46	14KJPN Submission ignored due to conflicting rows: Row 102911441 (NC_000015.10:30046079:A: 1532/28258) Row 102911442 (NC_000015.10:30046079::A 78/28258) Row 102911443 (NC_000015.10:30046079:AA: 2/28258)	-	Oct 16, 2022 (156)
47	14KJPN Submission ignored due to conflicting rows: Row 102911441 (NC_000015.10:30046079:A: 1532/28258) Row 102911442 (NC_000015.10:30046079::A 78/28258) Row 102911443 (NC_000015.10:30046079:AA: 2/28258)	-	Oct 16, 2022 (156)
48	ALFA	NC_000015.10 - 30046080	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs202086002	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
4421245663	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5215478805	NC_000015.9:30338282:AA:	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4286155952, ss5297911904, ss5769074339	NC_000015.10:30046079:AA:	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
4421245663	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss289248839	NC_000015.8:28125574:A:	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
479653, 14082554, ss1574838455, ss3013031173, ss3740797689, ss3787804430, ss3834162191, ss3840677842, ss5215478804	NC_000015.9:30338282:A:	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3846166615, ss4286155951, ss5297911902, ss5491713991, ss5769074337, ss5851232181	NC_000015.10:30046079:A:	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
4421245663	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss40538853	NT_010194.17:1128853:A:	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5215478803	NC_000015.9:30338282::A	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4286155946, ss5297911903, ss5491713992, ss5769074338	NC_000015.10:30046079::A	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
4421245663	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4286155947, ss5297911900, ss5491713993	NC_000015.10:30046079::AA	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
4421245663	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4286155948, ss5297911901, ss5491713994	NC_000015.10:30046079::AAA	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
4421245663	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4286155949	NC_000015.10:30046079::AAAA	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
4421245663	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4286155950	NC_000015.10:30046079::AAAAAAAAAAA… NC_000015.10:30046079::AAAAAAAAAAAAA	NC_000015.10:30046079:AAAAAAAAAAAA… NC_000015.10:30046079:AAAAAAAAAAAAAAA: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 rs35876784

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

rs35876784