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KCNQ1 c.387-21155C>T
Variant ID: 11-2528003-C-T
NM_000218.2(
KCNQ1
):c.387-21155C>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:
Evaluation of potential novel variations and their interactions related to bipolar disorders: analysis of genome-wide association study data.
Neuropsychiatric Disease And Treatment
Acikel, Cengizhan C; Aydin Son, Yesim Y; Celik, Cemil C; Gul, Husamettin H
Publication Date: 2016
Variant appearance in text: rs11023096
PubMed Link:
27920536
Variant Present in the following documents:
Main text
ndt-12-2997.pdf
View BVdb publication page