Bibliome.ai browser hg19
Search
About
Stats
FAQ
KYNU c.169+7666C>T
Variant ID: 2-143650771-C-T
NM_003937.2(
KYNU
):c.169+7666C>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:
Analyze multivariate phenotypes in genetic association studies by combining univariate association tests.
Genetic Epidemiology
Yang, Qiong Q; Wu, Hongsheng H; Guo, Chao-Yu CY; Fox, Caroline S CS
Publication Date: 2010-07
Variant appearance in text: rs16858223
PubMed Link:
20583287
Variant Present in the following documents:
Main text
View BVdb publication page