Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555103652
rs1555103652
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0424503
Disease:
Dysmorphic facies
C 0.700 GeneticVariation CLINVAR
dbSNP: rs886041095
rs886041095
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0424503
Disease:
Dysmorphic facies
T 0.700 GeneticVariation CLINVAR