Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518913
rs1057518913
EHMT1
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518913
rs1057518913
EHMT1
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		C 0.700 GeneticVariation CLINVAR