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: rs1555050158
rs1555050158
GRIA4
2 0.925 0.200 11 105926808 missense variant A/T snv 0.700 1.000 1 2017 2017
dbSNP: rs1555050165
rs1555050165
GRIA4
3 0.925 0.200 11 105926814 missense variant A/G snv 0.700 1.000 1 2017 2017
dbSNP: rs1555050171
rs1555050171
GRIA4
2 0.925 0.200 11 105926821 missense variant C/G snv 0.700 1.000 1 2017 2017
dbSNP: rs1555050174
rs1555050174
GRIA4
2 0.925 0.200 11 105926824 missense variant C/T snv 0.700 1.000 1 2017 2017