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SCN1A c.3429+2285A>G
Variant ID: 2-166890273-T-C
NM_001165963.1(
SCN1A
):c.3429+2285A>G
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.
The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04
Variant appearance in text: rs7571204
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Imputation-based analysis of association studies: candidate regions and quantitative traits.
Plos Genetics
Servin, Bertrand B; Stephens, Matthew M
Publication Date: 2007-07
Variant appearance in text: rs7571204
PubMed Link:
17676998
Variant Present in the following documents:
Main text
pgen.0030114.pdf
View BVdb publication page