FAS c.197-1244T>C

Variant ID: 10-90766213-T-C

NM_000043.4(FAS):c.197-1244T>C

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:

.

Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V
Publication Date: 2017

Variant appearance in text: rs7901656
PubMed Link: 32214685
Variant Present in the following documents:
  • 11825_2017_Article_126.pdf
View BVdb publication page