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NINJ2 c.34-41794C>G
Variant ID: 12-717138-G-C
NM_016533.6(
NINJ2
):c.34-41794C>G
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 fast multilocus test with adaptive SNP selection for large-scale genetic-association studies.
European Journal Of Human Genetics : Ejhg
Zhang, Han H; Shi, Jianxin J; Liang, Faming F; Wheeler, William W; Stolzenberg-Solomon, Rachael R; Yu, Kai K
Publication Date: 2014-05
Variant appearance in text: rs2075032
PubMed Link:
24022295
Variant Present in the following documents:
Main text
View BVdb publication page