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.




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