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: rs786205232
rs786205232
KCNA2
5 0.925 0.040 1 110603893 missense variant C/T snv 4.0E-06 0.800 1.000 3 2015 2016
dbSNP: rs876657389
rs876657389
KCNA2
1 1.000 0.040 1 110603569 missense variant G/A snv 0.800 1.000 2 2015 2015
dbSNP: rs876657390
rs876657390
KCNA2
1 1.000 0.040 1 110603889 missense variant C/A snv 0.800 1.000 2 2015 2015
dbSNP: rs786205231
rs786205231
KCNA2
1 1.000 0.040 1 110603995 missense variant A/G snv 0.800 0
dbSNP: rs886041761
rs886041761
KCNA2
6 0.925 0.200 1 110603902 missense variant C/T snv 0.700 1.000 2 2016 2017
dbSNP: rs763353895
rs763353895
KCNA2
1 1.000 0.040 1 110604590 stop gained G/A snv 4.0E-06 0.700 1.000 1 2017 2017
dbSNP: rs1064794738
rs1064794738
KCNA2
1 1.000 0.040 1 110603588 missense variant C/T snv 0.700 0
dbSNP: rs1553181280
rs1553181280
KCNA2
1 1.000 0.040 1 110603663 missense variant T/C snv 0.700 0
dbSNP: rs1553181282
rs1553181282
KCNA2
1 1.000 0.040 1 110603665 missense variant G/A snv 0.700 0
dbSNP: rs1553181301
rs1553181301
KCNA2
1 1.000 0.040 1 110603770 missense variant C/T snv 0.700 0
dbSNP: rs1553181323
rs1553181323
KCNA2
1 1.000 0.040 1 110603824 missense variant G/A snv 0.700 0