Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs770913157
rs770913157
G 0.700 CausalMutation CLINVAR Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. 26974950

2016

dbSNP: rs869312829
rs869312829
G 0.700 CausalMutation CLINVAR Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. 26974950

2016

dbSNP: rs869312830
rs869312830
A 0.700 CausalMutation CLINVAR Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. 26974950

2016

dbSNP: rs869312831
rs869312831
T 0.700 CausalMutation CLINVAR Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. 26974950

2016

dbSNP: rs869312832
rs869312832
GC 0.700 CausalMutation CLINVAR Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. 26974950

2016