Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894722
rs104894722
TGFB1
CUI: C0011989
Disease: Camurati-Engelmann Syndrome
Camurati-Engelmann Syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs104894722
rs104894722
TGFB1
CUI: C0011989
Disease: Camurati-Engelmann Syndrome
Camurati-Engelmann Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs104894722
rs104894722
TGFB1
CUI: C0011989
Disease: Camurati-Engelmann Syndrome
Camurati-Engelmann Syndrome 		G 0.700 CausalMutation CLINVAR