IFT172 c.39+74G>A

Variant ID: 2-27712408-C-T

NM_015662.1(IFT172):c.39+74G>A

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:

JAM: A Scalable Bayesian Framework for Joint Analysis of Marginal SNP Effects.

Genetic Epidemiology
Newcombe, Paul J PJ; Conti, David V DV; Richardson, Sylvia S
Publication Date: 2016-04

Variant appearance in text: rs7583698
PubMed Link: 27027514
Variant Present in the following documents:
  • GEPI-40-188-s001.pdf
View BVdb publication page