Name: rs1491336154
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.

rs1491336154

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:34751954-34751955 (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: insA / insAA / insAAA / ins(A)₄ / …
insA / insAA / insAAA / ins(A)₄ / ins(A)₅ / ins(A)₆ / ins(A)₇ / ins(A)₈ / ins(A)₉ / ins(A)₁₀ / ins(A)₁₁ / ins(A)₁₂ / ins(A)₁₃ / ins(A)₁₄ / ins(A)₁₅ / ins(A)₁₆ / ins(A)₁₈ / ins(A)₂₀ / ins(A)₃₅ / ins(A)₃₈ / ins(A)₂₀C(A)₆ / ins(A)₈C(A)₁₂ / ins(A)₇GAA / ins(A)₇GAAA / ins(A)₇G(A)₄
Variation Type: Insertion
Frequency: insAA=0.000004 (1/264690, TOPMED)
insA=0.00000 (0/11860, ALFA)
insAA=0.00000 (0/11860, ALFA) (+ 19 more)
insAAA=0.00000 (0/11860, ALFA)
ins(A)₄=0.00000 (0/11860, ALFA)
ins(A)₅=0.00000 (0/11860, ALFA)
ins(A)₆=0.00000 (0/11860, ALFA)
ins(A)₇=0.00000 (0/11860, ALFA)
ins(A)₈=0.00000 (0/11860, ALFA)
ins(A)₉=0.00000 (0/11860, ALFA)
ins(A)₁₀=0.00000 (0/11860, ALFA)
ins(A)₁₁=0.00000 (0/11860, ALFA)
ins(A)₁₂=0.00000 (0/11860, ALFA)
ins(A)₁₃=0.00000 (0/11860, ALFA)
ins(A)₁₄=0.00000 (0/11860, ALFA)
ins(A)₁₅=0.00000 (0/11860, ALFA)
ins(A)₁₆=0.00000 (0/11860, ALFA)
ins(A)₁₈=0.00000 (0/11860, ALFA)
ins(A)₇GAA=0.00000 (0/11860, ALFA)
ins(A)₇GAAA=0.00000 (0/11860, ALFA)
ins(A)₇G(A)₄=0.00000 (0/11860, ALFA)
ins(A)₂₀=0.038 (5/130, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GJD2 : 3 Prime UTR 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	11860	=1.00000	A=0.00000, AA=0.00000, AAA=0.00000, AAAA=0.00000, AAAAA=0.00000, AAAAAA=0.00000, AAAAAAA=0.00000, AAAAAAAA=0.00000, AAAAAAAAA=0.00000, AAAAAAAAAA=0.00000, AAAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAGAA=0.00000, AAAAAAAGAAA=0.00000, AAAAAAAGAAAA=0.00000	1.0	N/A
European	Sub	7618	=1.0000	A=0.0000, AA=0.0000, AAA=0.0000, AAAA=0.0000, AAAAA=0.0000, AAAAAA=0.0000, AAAAAAA=0.0000, AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAGAA=0.0000, AAAAAAAGAAA=0.0000, AAAAAAAGAAAA=0.0000	1.0	N/A
African	Sub	2814	=1.0000	A=0.0000, AA=0.0000, AAA=0.0000, AAAA=0.0000, AAAAA=0.0000, AAAAAA=0.0000, AAAAAAA=0.0000, AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAGAA=0.0000, AAAAAAAGAAA=0.0000, AAAAAAAGAAAA=0.0000	1.0	N/A
African Others	Sub	108	=1.000	A=0.000, AA=0.000, AAA=0.000, AAAA=0.000, AAAAA=0.000, AAAAAA=0.000, AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAGAA=0.000, AAAAAAAGAAA=0.000, AAAAAAAGAAAA=0.000	1.0	N/A
African American	Sub	2706	=1.0000	A=0.0000, AA=0.0000, AAA=0.0000, AAAA=0.0000, AAAAA=0.0000, AAAAAA=0.0000, AAAAAAA=0.0000, AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAGAA=0.0000, AAAAAAAGAAA=0.0000, AAAAAAAGAAAA=0.0000	1.0	N/A
Asian	Sub	108	=1.000	A=0.000, AA=0.000, AAA=0.000, AAAA=0.000, AAAAA=0.000, AAAAAA=0.000, AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAGAA=0.000, AAAAAAAGAAA=0.000, AAAAAAAGAAAA=0.000	1.0	N/A
East Asian	Sub	84	=1.00	A=0.00, AA=0.00, AAA=0.00, AAAA=0.00, AAAAA=0.00, AAAAAA=0.00, AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAGAA=0.00, AAAAAAAGAAA=0.00, AAAAAAAGAAAA=0.00	1.0	N/A
Other Asian	Sub	24	=1.00	A=0.00, AA=0.00, AAA=0.00, AAAA=0.00, AAAAA=0.00, AAAAAA=0.00, AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAGAA=0.00, AAAAAAAGAAA=0.00, AAAAAAAGAAAA=0.00	1.0	N/A
Latin American 1	Sub	146	=1.000	A=0.000, AA=0.000, AAA=0.000, AAAA=0.000, AAAAA=0.000, AAAAAA=0.000, AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAGAA=0.000, AAAAAAAGAAA=0.000, AAAAAAAGAAAA=0.000	1.0	N/A
Latin American 2	Sub	610	=1.000	A=0.000, AA=0.000, AAA=0.000, AAAA=0.000, AAAAA=0.000, AAAAAA=0.000, AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAGAA=0.000, AAAAAAAGAAA=0.000, AAAAAAAGAAAA=0.000	1.0	N/A
South Asian	Sub	94	=1.00	A=0.00, AA=0.00, AAA=0.00, AAAA=0.00, AAAAA=0.00, AAAAAA=0.00, AAAAAAA=0.00, AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAGAA=0.00, AAAAAAAGAAA=0.00, AAAAAAAGAAAA=0.00	1.0	N/A
Other	Sub	470	=1.000	A=0.000, AA=0.000, AAA=0.000, AAAA=0.000, AAAAA=0.000, AAAAAA=0.000, AAAAAAA=0.000, AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAGAA=0.000, AAAAAAAGAAA=0.000, AAAAAAAGAAAA=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
TopMed	Global	Study-wide	264690	- No frequency provided	insAA=0.000004
Allele Frequency Aggregator	Total	Global	11860	- No frequency provided	insA=0.00000, insAA=0.00000, insAAA=0.00000, ins(A)₄=0.00000, ins(A)₅=0.00000, ins(A)₆=0.00000, ins(A)₇=0.00000, ins(A)₈=0.00000, ins(A)₉=0.00000, ins(A)₁₀=0.00000, ins(A)₁₁=0.00000, ins(A)₁₂=0.00000, ins(A)₁₃=0.00000, ins(A)₁₄=0.00000, ins(A)₁₅=0.00000, ins(A)₁₆=0.00000, ins(A)₁₈=0.00000, ins(A)₇GAA=0.00000, ins(A)₇GAAA=0.00000, ins(A)₇G(A)₄=0.00000
Allele Frequency Aggregator	European	Sub	7618	- No frequency provided	insA=0.0000, insAA=0.0000, insAAA=0.0000, ins(A)₄=0.0000, ins(A)₅=0.0000, ins(A)₆=0.0000, ins(A)₇=0.0000, ins(A)₈=0.0000, ins(A)₉=0.0000, ins(A)₁₀=0.0000, ins(A)₁₁=0.0000, ins(A)₁₂=0.0000, ins(A)₁₃=0.0000, ins(A)₁₄=0.0000, ins(A)₁₅=0.0000, ins(A)₁₆=0.0000, ins(A)₁₈=0.0000, ins(A)₇GAA=0.0000, ins(A)₇GAAA=0.0000, ins(A)₇G(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	2814	- No frequency provided	insA=0.0000, insAA=0.0000, insAAA=0.0000, ins(A)₄=0.0000, ins(A)₅=0.0000, ins(A)₆=0.0000, ins(A)₇=0.0000, ins(A)₈=0.0000, ins(A)₉=0.0000, ins(A)₁₀=0.0000, ins(A)₁₁=0.0000, ins(A)₁₂=0.0000, ins(A)₁₃=0.0000, ins(A)₁₄=0.0000, ins(A)₁₅=0.0000, ins(A)₁₆=0.0000, ins(A)₁₈=0.0000, ins(A)₇GAA=0.0000, ins(A)₇GAAA=0.0000, ins(A)₇G(A)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	- No frequency provided	insA=0.000, insAA=0.000, insAAA=0.000, ins(A)₄=0.000, ins(A)₅=0.000, ins(A)₆=0.000, ins(A)₇=0.000, ins(A)₈=0.000, ins(A)₉=0.000, ins(A)₁₀=0.000, ins(A)₁₁=0.000, ins(A)₁₂=0.000, ins(A)₁₃=0.000, ins(A)₁₄=0.000, ins(A)₁₅=0.000, ins(A)₁₆=0.000, ins(A)₁₈=0.000, ins(A)₇GAA=0.000, ins(A)₇GAAA=0.000, ins(A)₇G(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	470	- No frequency provided	insA=0.000, insAA=0.000, insAAA=0.000, ins(A)₄=0.000, ins(A)₅=0.000, ins(A)₆=0.000, ins(A)₇=0.000, ins(A)₈=0.000, ins(A)₉=0.000, ins(A)₁₀=0.000, ins(A)₁₁=0.000, ins(A)₁₂=0.000, ins(A)₁₃=0.000, ins(A)₁₄=0.000, ins(A)₁₅=0.000, ins(A)₁₆=0.000, ins(A)₁₈=0.000, ins(A)₇GAA=0.000, ins(A)₇GAAA=0.000, ins(A)₇G(A)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	- No frequency provided	insA=0.000, insAA=0.000, insAAA=0.000, ins(A)₄=0.000, ins(A)₅=0.000, ins(A)₆=0.000, ins(A)₇=0.000, ins(A)₈=0.000, ins(A)₉=0.000, ins(A)₁₀=0.000, ins(A)₁₁=0.000, ins(A)₁₂=0.000, ins(A)₁₃=0.000, ins(A)₁₄=0.000, ins(A)₁₅=0.000, ins(A)₁₆=0.000, ins(A)₁₈=0.000, ins(A)₇GAA=0.000, ins(A)₇GAAA=0.000, ins(A)₇G(A)₄=0.000
Allele Frequency Aggregator	Asian	Sub	108	- No frequency provided	insA=0.000, insAA=0.000, insAAA=0.000, ins(A)₄=0.000, ins(A)₅=0.000, ins(A)₆=0.000, ins(A)₇=0.000, ins(A)₈=0.000, ins(A)₉=0.000, ins(A)₁₀=0.000, ins(A)₁₁=0.000, ins(A)₁₂=0.000, ins(A)₁₃=0.000, ins(A)₁₄=0.000, ins(A)₁₅=0.000, ins(A)₁₆=0.000, ins(A)₁₈=0.000, ins(A)₇GAA=0.000, ins(A)₇GAAA=0.000, ins(A)₇G(A)₄=0.000
Allele Frequency Aggregator	South Asian	Sub	94	- No frequency provided	insA=0.00, insAA=0.00, insAAA=0.00, ins(A)₄=0.00, ins(A)₅=0.00, ins(A)₆=0.00, ins(A)₇=0.00, ins(A)₈=0.00, ins(A)₉=0.00, ins(A)₁₀=0.00, ins(A)₁₁=0.00, ins(A)₁₂=0.00, ins(A)₁₃=0.00, ins(A)₁₄=0.00, ins(A)₁₅=0.00, ins(A)₁₆=0.00, ins(A)₁₈=0.00, ins(A)₇GAA=0.00, ins(A)₇GAAA=0.00, ins(A)₇G(A)₄=0.00
Northern Sweden	ACPOP	Study-wide	130	- No frequency provided	ins(A)₂₀=0.038

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.34751954_34751955insA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAAAAAAACAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAACAAAAAAAAAAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAGAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAGAAA
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955insAAAAAAAGAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAAAAAAACAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAACAAAAAAAAAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAGAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAGAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156insAAAAAAAGAAAA

Gene: GJD2, gap junction protein delta 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GJD2 transcript	NM_020660.3:c.523_524=	N/A	3 Prime UTR Variant
GJD2 transcript variant X1	XM_017022438.2:c.523_52… XM_017022438.2:c.523_524=	N/A	3 Prime UTR 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	=	insA	insAA	insAAA	ins(A)₄	ins(A)₅	ins(A)₆	ins(A)₇	ins(A)₈	ins(A)₉	ins(A)₁₀	ins(A)₁₁	ins(A)₁₂	ins(A)₁₃	ins(A)₁₄	ins(A)₁₅	ins(A)₁₆	ins(A)₁₈	ins(A)₂₀	ins(A)₃₅	ins(A)₃₈	ins(A)₂₀C(A)₆	ins(A)₈C(A)₁₂	ins(A)₇GAA	ins(A)₇GAAA	ins(A)₇G(A)₄
GRCh38.p14 chr 15	NC_000015.10:g.34751954_34751955=	NC_000015.10:g.34751954_34751955insA	NC_000015.10:g.34751954_34751955insAA	NC_000015.10:g.34751954_34751955insAAA	NC_000015.10:g.34751954_34751955insAAAA	NC_000015.10:g.34751954_34751955insAAAAA	NC_000015.10:g.34751954_34751955insAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAAAAAAAAAAAAAACAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAACAAAAAAAAAAAA	NC_000015.10:g.34751954_34751955insAAAAAAAGAA	NC_000015.10:g.34751954_34751955insAAAAAAAGAAA	NC_000015.10:g.34751954_34751955insAAAAAAAGAAAA
GRCh37.p13 chr 15	NC_000015.9:g.35044155_35044156=	NC_000015.9:g.35044155_35044156insA	NC_000015.9:g.35044155_35044156insAA	NC_000015.9:g.35044155_35044156insAAA	NC_000015.9:g.35044155_35044156insAAAA	NC_000015.9:g.35044155_35044156insAAAAA	NC_000015.9:g.35044155_35044156insAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAAAAAAAAAAAAAACAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAACAAAAAAAAAAAA	NC_000015.9:g.35044155_35044156insAAAAAAAGAA	NC_000015.9:g.35044155_35044156insAAAAAAAGAAA	NC_000015.9:g.35044155_35044156insAAAAAAAGAAAA
GJD2 transcript	NM_020660.3:c.523_524=	NM_020660.3:c.523_524insT	NM_020660.3:c.523_524insTT	NM_020660.3:c.523_524insTTT	NM_020660.3:c.523_524insTTTT	NM_020660.3:c.523_524insTTTTT	NM_020660.3:c.523_524insTTTTTT	NM_020660.3:c.523_524insTTTTTTT	NM_020660.3:c.523_524insTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTTTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTTTTTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTGTTTTTTTTTTTTTTTTTTTT	NM_020660.3:c.523_524insTTTTTTTTTTTTGTTTTTTTT	NM_020660.3:c.523_524insTTCTTTTTTT	NM_020660.3:c.523_524insTTTCTTTTTTT	NM_020660.3:c.523_524insTTTTCTTTTTTT
GJD2 transcript variant X1	XM_017022438.2:c.523_524=	XM_017022438.2:c.523_524insT	XM_017022438.2:c.523_524insTT	XM_017022438.2:c.523_524insTTT	XM_017022438.2:c.523_524insTTTT	XM_017022438.2:c.523_524insTTTTT	XM_017022438.2:c.523_524insTTTTTT	XM_017022438.2:c.523_524insTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTTTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTTTTTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTGTTTTTTTTTTTTTTTTTTTT	XM_017022438.2:c.523_524insTTTTTTTTTTTTGTTTTTTTT	XM_017022438.2:c.523_524insTTCTTTTTTT	XM_017022438.2:c.523_524insTTTCTTTTTTT	XM_017022438.2:c.523_524insTTTTCTTTTTTT
GJD2 transcript variant X1	XM_017022438.1:c.523_524=	XM_017022438.1:c.523_524insT	XM_017022438.1:c.523_524insTT	XM_017022438.1:c.523_524insTTT	XM_017022438.1:c.523_524insTTTT	XM_017022438.1:c.523_524insTTTTT	XM_017022438.1:c.523_524insTTTTTT	XM_017022438.1:c.523_524insTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTTTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTTTTTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTGTTTTTTTTTTTTTTTTTTTT	XM_017022438.1:c.523_524insTTTTTTTTTTTTGTTTTTTTT	XM_017022438.1:c.523_524insTTCTTTTTTT	XM_017022438.1:c.523_524insTTTCTTTTTTT	XM_017022438.1:c.523_524insTTTTCTTTTTTT

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#.

19 SubSNP, 13 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3697665854	Jul 13, 2019 (153)
2	EVA_DECODE	ss3697665855	Jul 13, 2019 (153)
3	EVA_DECODE	ss3697665856	Jul 13, 2019 (153)
4	ACPOP	ss3740826015	Jul 13, 2019 (153)
5	GNOMAD	ss4286680948	Apr 26, 2021 (155)
6	GNOMAD	ss4286680949	Apr 26, 2021 (155)
7	GNOMAD	ss4286680950	Apr 26, 2021 (155)
8	GNOMAD	ss4286680951	Apr 26, 2021 (155)
9	GNOMAD	ss4286680952	Apr 26, 2021 (155)
10	TOPMED	ss4987154621	Apr 26, 2021 (155)
11	TOMMO_GENOMICS	ss5215641549	Apr 26, 2021 (155)
12	TOMMO_GENOMICS	ss5215641550	Apr 26, 2021 (155)
13	TOMMO_GENOMICS	ss5215641551	Apr 26, 2021 (155)
14	1000G_HIGH_COVERAGE	ss5298027840	Oct 16, 2022 (156)
15	HUGCELL_USP	ss5491801657	Oct 16, 2022 (156)
16	HUGCELL_USP	ss5491801658	Oct 16, 2022 (156)
17	TOMMO_GENOMICS	ss5769281995	Oct 16, 2022 (156)
18	TOMMO_GENOMICS	ss5769281999	Oct 16, 2022 (156)
19	EVA	ss5828045091	Oct 16, 2022 (156)
20	gnomAD - Genomes Submission ignored due to conflicting rows: Row 465563567 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAA 35/30994) Row 465563568 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 4/30996) Row 465563569 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 1/30996)...	-	Apr 26, 2021 (155)
21	gnomAD - Genomes Submission ignored due to conflicting rows: Row 465563567 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAA 35/30994) Row 465563568 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 4/30996) Row 465563569 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 1/30996)...	-	Apr 26, 2021 (155)
22	gnomAD - Genomes Submission ignored due to conflicting rows: Row 465563567 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAA 35/30994) Row 465563568 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 4/30996) Row 465563569 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 1/30996)...	-	Apr 26, 2021 (155)
23	gnomAD - Genomes Submission ignored due to conflicting rows: Row 465563567 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAA 35/30994) Row 465563568 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 4/30996) Row 465563569 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 1/30996)...	-	Apr 26, 2021 (155)
24	gnomAD - Genomes Submission ignored due to conflicting rows: Row 465563567 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAA 35/30994) Row 465563568 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 4/30996) Row 465563569 (NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 1/30996)...	-	Apr 26, 2021 (155)
25	Northern Sweden	NC_000015.9 - 35044156	Jul 13, 2019 (153)
26	8.3KJPN Submission ignored due to conflicting rows: Row 73610856 (NC_000015.9:35044155::AA 886/15396) Row 73610857 (NC_000015.9:35044155::AAAAAAAAAAAAAA 395/15396) Row 73610858 (NC_000015.9:35044155::AAAAAAAAAAAAAAA 449/15396)	-	Apr 26, 2021 (155)
27	8.3KJPN Submission ignored due to conflicting rows: Row 73610856 (NC_000015.9:35044155::AA 886/15396) Row 73610857 (NC_000015.9:35044155::AAAAAAAAAAAAAA 395/15396) Row 73610858 (NC_000015.9:35044155::AAAAAAAAAAAAAAA 449/15396)	-	Apr 26, 2021 (155)
28	8.3KJPN Submission ignored due to conflicting rows: Row 73610856 (NC_000015.9:35044155::AA 886/15396) Row 73610857 (NC_000015.9:35044155::AAAAAAAAAAAAAA 395/15396) Row 73610858 (NC_000015.9:35044155::AAAAAAAAAAAAAAA 449/15396)	-	Apr 26, 2021 (155)
29	14KJPN Submission ignored due to conflicting rows: Row 103119099 (NC_000015.10:34751954::AA 1660/24220) Row 103119103 (NC_000015.10:34751954::AAAAAAAAAAAAAAA 811/24220)	-	Oct 16, 2022 (156)
30	14KJPN Submission ignored due to conflicting rows: Row 103119099 (NC_000015.10:34751954::AA 1660/24220) Row 103119103 (NC_000015.10:34751954::AAAAAAAAAAAAAAA 811/24220)	-	Oct 16, 2022 (156)
31	TopMed	NC_000015.10 - 34751955	Apr 26, 2021 (155)
32	ALFA	NC_000015.10 - 34751955	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:

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

No publications for rs1491336154

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

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
14131253735	NC_000015.10:34751954::A	NC_000015.10:34751954::A	(self)
ss5215641549, ss5828045091	NC_000015.9:35044155::AA	NC_000015.10:34751954::AA	(self)
202700281, 14131253735, ss4987154621, ss5298027840, ss5769281995	NC_000015.10:34751954::AA	NC_000015.10:34751954::AA	(self)
14131253735, ss5491801658	NC_000015.10:34751954::AAA	NC_000015.10:34751954::AAA	(self)
14131253735, ss3697665856	NC_000015.10:34751954::AAAA	NC_000015.10:34751954::AAAA	(self)
14131253735	NC_000015.10:34751954::AAAAA	NC_000015.10:34751954::AAAAA	(self)
14131253735	NC_000015.10:34751954::AAAAAA	NC_000015.10:34751954::AAAAAA	(self)
14131253735	NC_000015.10:34751954::AAAAAAA	NC_000015.10:34751954::AAAAAAA	(self)
14131253735	NC_000015.10:34751954::AAAAAAAA	NC_000015.10:34751954::AAAAAAAA	(self)
14131253735	NC_000015.10:34751954::AAAAAAAAA	NC_000015.10:34751954::AAAAAAAAA	(self)
14131253735	NC_000015.10:34751954::AAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAA	(self)
14131253735	NC_000015.10:34751954::AAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA	(self)
14131253735	NC_000015.10:34751954::AAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAAA	(self)
14131253735, ss3697665855	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAA	(self)
ss5215641550	NC_000015.9:35044155::AAAAAAAAAAAA… NC_000015.9:35044155::AAAAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAA	(self)
14131253735, ss3697665854	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAA	(self)
ss5215641551	NC_000015.9:35044155::AAAAAAAAAAAA… NC_000015.9:35044155::AAAAAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAA	(self)
14131253735, ss5769281999	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAA	(self)
14131253735, ss5491801657	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAA	(self)
14131253735	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAAAA	(self)
14110880, ss3740826015	NC_000015.9:35044155::AAAAAAAAAAAA… NC_000015.9:35044155::AAAAAAAAAAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAA	(self)
ss4286680948	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAA	(self)
ss4286680949	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4286680950	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4286680951	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAACAAAAAA	NC_000015.10:34751954::AAAAAAAAAAA… NC_000015.10:34751954::AAAAAAAAAAAAAAAAAAAACAAAAAA	(self)
ss4286680952	NC_000015.10:34751954::AAAAAAAACAA… NC_000015.10:34751954::AAAAAAAACAAAAAAAAAAAA	NC_000015.10:34751954::AAAAAAAACAA… NC_000015.10:34751954::AAAAAAAACAAAAAAAAAAAA	(self)
14131253735	NC_000015.10:34751954::AAAAAAAGAA	NC_000015.10:34751954::AAAAAAAGAA	(self)
14131253735	NC_000015.10:34751954::AAAAAAAGAAA	NC_000015.10:34751954::AAAAAAAGAAA	(self)
14131253735	NC_000015.10:34751954::AAAAAAAGAAAA	NC_000015.10:34751954::AAAAAAAGAAAA	(self)

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491336154