EHD1 c.502+3852G>T

Variant ID: 11-64638041-C-A

NM_006795.2(EHD1):c.502+3852G>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:

RAPID detection of gene-gene interactions in genome-wide association studies.

Bioinformatics (Oxford, England)
Brinza, Dumitru D; Schultz, Matthew M; Tesler, Glenn G; Bafna, Vineet V
Publication Date: 2010-11-15

Variant appearance in text: rs17146413
PubMed Link: 20871107
Variant Present in the following documents:
  • Main text
View BVdb publication page