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SLC22A1 c.1386-684C>A
Variant ID: 6-160575146-C-A
NM_003057.2(
SLC22A1
):c.1386-684C>A
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:
Association Study of Puberty-Related Candidate Genes in Chinese Female Population.
International Journal Of Genomics
Omariba, Gideon G; Xiao, Junhua J
Publication Date: 2020
Variant appearance in text: rs9347389
PubMed Link:
32566640
Variant Present in the following documents:
Main text
IJG2020-1426761.pdf
View BVdb publication page
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: rs9347389
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page