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CLCN6 c.1248+1316C>T
Variant ID: 1-11890695-C-T
NM_001286.3(
CLCN6
):c.1248+1316C>T
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
A multiple coefficient of determination-based method for parsing SNPs that correlate with mRNA expression.
Scientific Reports
Song, Fan F; Tao, Yu Y; Sun, Yue Y; Saffen, David D
Publication Date: 2019-12-27
Variant appearance in text: rs503040
PubMed Link:
31882953
Variant Present in the following documents:
41598_2019_56494_MOESM1_ESM.pdf
View BVdb publication page