MYOF c.236+9123C>G

Variant ID: 10-95202684-G-C

NM_013451.3(MYOF):c.236+9123C>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:

Distinct clinical phenotypes for Crohn's disease derived from patient surveys.

Bmc Gastroenterology
Liu, Tianyun T; Han, Lichy L; Tilley, Mera M; Afzelius, Lovisa L; Maciejewski, Mateusz M; Jelinsky, Scott S; Tian, Chao C; McIntyre, Matthew M; , ; Bing, Nan N; Hung, Kenneth K; Altman, Russ B RB
Publication Date: 2021-04-09

Variant appearance in text: rs75506868
PubMed Link: 33836648
Variant Present in the following documents:
  • Main text
  • 12876_2021_Article_1740.pdf
View BVdb publication page