Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057523157
rs1057523157
SETD2
CUI: C4085873
Disease: LUSCAN-LUMISH SYNDROME
LUSCAN-LUMISH SYNDROME 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057523157
rs1057523157
SETD2
CUI: C4085873
Disease: LUSCAN-LUMISH SYNDROME
LUSCAN-LUMISH SYNDROME 		A 0.700 CausalMutation CLINVAR