Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886041095
GRIN2B
0.827 0.160 12 13571930 missense variant C/T snv 11
rs876661151
LOC105369668 ; GRIN2B
0.925 0.040 12 13608611 missense variant C/A;T snv 6