rs876661219, GRIN2B

N. diseases: 2
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 1.000 12 13571891 missense variant A/C;G snv 0.700 0
Mental impairment
CUI: C0683322
Disease: Mental impairment
14 1.000 12 13571891 missense variant A/C;G snv 0.700 0