Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs146539065
rs146539065
Entrez Id: 51091
Gene Symbol: SEPSECS
SEPSECS
CUI: C0344482
Disease:
Hypoplasia of corpus callosum
T 0.700 GeneticVariation CLINVAR
dbSNP: rs776969714
rs776969714
Entrez Id: 51091
Gene Symbol: SEPSECS
SEPSECS
CUI: C0344482
Disease:
Hypoplasia of corpus callosum
GC 0.700 CausalMutation CLINVAR