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: rs193929356
rs193929356
KCNJ11
4 0.925 0.080 11 17387103 missense variant T/A;C snv 0.700 0
dbSNP: rs587783670
rs587783670
KCNJ11
1 11 17387571 missense variant G/C;T snv 0.700 0
dbSNP: rs587783671
rs587783671
KCNJ11
1 11 17387556 missense variant T/G snv 0.700 0
dbSNP: rs587783674
rs587783674
KCNJ11
1 11 17388084 missense variant G/C snv 0.700 0
dbSNP: rs80356616
rs80356616
KCNJ11
19 0.732 0.360 11 17387917 missense variant C/T snv 0.700 0
dbSNP: rs80356624
rs80356624
KCNJ11
16 0.752 0.240 11 17387490 missense variant C/A;T snv 0.700 0