Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1559751245
rs1559751245
MITF
CUI: C0162835
Disease: Hypopigmentation disorder
Hypopigmentation disorder 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs28940877
rs28940877
TYR ; LOC107984363
CUI: C0162835
Disease: Hypopigmentation disorder
Hypopigmentation disorder 		C 0.700 CausalMutation CLINVAR

dbSNP: rs28940881
rs28940881
TYR ; LOC107984363
CUI: C0162835
Disease: Hypopigmentation disorder
Hypopigmentation disorder 		G 0.700 CausalMutation CLINVAR

dbSNP: rs376823382
rs376823382
TYR ; LOC107984363
CUI: C0162835
Disease: Hypopigmentation disorder
Hypopigmentation disorder 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs587777893
rs587777893
MTOR
CUI: C0162835
Disease: Hypopigmentation disorder
Hypopigmentation disorder 		A 0.700 CausalMutation CLINVAR

dbSNP: rs879255280
rs879255280
SMO
CUI: C0162835
Disease: Hypopigmentation disorder
Hypopigmentation disorder 		T 0.700 CausalMutation CLINVAR