HNF4A c.361A>G ;(p.S121G)

Variant ID: 20-43042375-A-G

NM_175914.4(HNF4A):c.361A>G;(p.S121G)

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:

Statistical evidence for high-penetrance MODY-causing genes in a large population-based cohort.

Endocrinology, Diabetes & Metabolism
Billings, Liana K LK; Shi, Zhuqing Z; Resurreccion, W Kyle WK; Wang, Chi-Hsiung CH; Wei, Jun J; Pollin, Toni I TI; Udler, Miriam S MS; Xu, Jianfeng J
Publication Date: 2022-11

Variant appearance in text: HNF4A: S121G; rs193922472
PubMed Link: 36208030
Variant Present in the following documents:
  • EDM2-5-e372-s001.xlsx, sheet 1
View BVdb publication page