MEGF9 c.601+22755A>G

Variant ID: 9-123453281-T-C

NM_001080497.2(MEGF9):c.601+22755A>G

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:

Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families.

European Journal Of Human Genetics : Ejhg
Mustonen, Tuuli T; Schmidt, Eeva-Kaisa EK; Valori, Miko M; Tienari, Pentti J PJ; Atula, Sari S; Kiuru-Enari, Sari S
Publication Date: 2018-01

Variant appearance in text: rs966396
PubMed Link: 29167514
Variant Present in the following documents:
  • Main text
View BVdb publication page