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VWF c.2626C>T ;(p.L876F)
Variant ID: 12-6143913-G-A
NM_000552.3(
VWF
):c.2626C>T;(p.L876F)
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: Leu876Phe; rs143762054
PubMed Link:
26420797
Variant Present in the following documents:
Main text
View BVdb publication page