Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1163944538
rs1163944538
Entrez Id: 9772
Gene Symbol: TMEM94
TMEM94
CUI: C4025790
Disease:
Specific learning disability
GA 0.700 CausalMutation CLINVAR
dbSNP: rs1352010373
rs1352010373
Entrez Id: 9772
Gene Symbol: TMEM94
TMEM94
CUI: C4025790
Disease:
Specific learning disability
C 0.700 CausalMutation CLINVAR