Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs886040861
rs886040861
GRIN2D
2 0.925 0.040 19 48419722 missense variant G/A snv 0.800 1.000 1 2016 2016
dbSNP: rs1569064110
rs1569064110
GRIN2D
1 1.000 19 48414517 missense variant G/A snv 0.700 0
dbSNP: rs1569065861
rs1569065861
GRIN2D
1 1.000 19 48419766 missense variant G/C snv 0.700 0
dbSNP: rs1569065866
rs1569065866
GRIN2D
1 1.000 19 48419803 missense variant A/C snv 0.700 0