VWF c.409G>T ;(p.V137L)

Variant ID: 12-6219663-C-A

NM_000552.3(VWF):c.409G>T;(p.V137L)

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:

Group association test using a hidden Markov model.

Biostatistics (Oxford, England)
Cheng, Yichen Y; Dai, James Y JY; Kooperberg, Charles C
Publication Date: 2016-04

Variant appearance in text: VWF: Val137Leu; rs71582882
PubMed Link: 26420797
Variant Present in the following documents:
  • Main text
View BVdb publication page