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: rs137852350
rs137852350
GRIA3
1 1.000 0.080 X 123482856 missense variant G/A snv 0.800 0
dbSNP: rs137852351
rs137852351
GRIA3
2 0.925 0.080 X 123427954 missense variant C/A snv 0.800 0
dbSNP: rs137852352
rs137852352
GRIA3
1 1.000 0.080 X 123464905 missense variant T/C snv 0.800 0
dbSNP: rs1057521721
rs1057521721
GRIA3
5 0.851 0.200 X 123428020 missense variant G/A snv 0.700 0
dbSNP: rs1135401788
rs1135401788
GRIA3
1 1.000 0.080 X 123428027 missense variant T/C snv 0.700 0
dbSNP: rs368568228
rs368568228
GRIA3
2 0.925 0.080 X 123404763 missense variant G/A snv 2.7E-05 2.8E-05 0.700 0
dbSNP: rs587777361
rs587777361
GRIA3
1 1.000 0.080 X 123427951 missense variant G/C snv 0.700 0