rs1057518988, GRIN2B

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Ataxia
CUI: C0004134
Disease: Ataxia
68 0.925 0.040 12 13571859 missense variant T/C snv 0.700 0
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.925 0.040 12 13571859 missense variant T/C snv 0.700 0
Mental impairment
CUI: C0683322
Disease: Mental impairment
14 0.925 0.040 12 13571859 missense variant T/C snv 0.700 0