Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs876661335
rs876661335
Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
CUI: C0079541
Disease:
Holoprosencephaly
T 0.700 GeneticVariation CLINVAR