Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853214
rs137853214
Entrez Id: 902;5921
Gene Symbol: CCNH;RASA1
CCNH;RASA1
CUI: C3838465
Disease:
BASAL CELL CARCINOMA, SOMATIC
T 0.700 CausalMutation CLINVAR