Disease: MIGRAINE, FAMILIAL HEMIPLEGIC, 2
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs746795369
ATP1A2
0.827 0.080 1 160139969 missense variant C/A;T snv 1.2E-05; 4.0E-06 6
rs28933400
ATP1A2
0.882 0.080 1 160135510 missense variant T/C snv 3
rs28933401
ATP1A2
0.882 0.120 1 160135246 missense variant G/A snv 3
rs121918613
ATP1A2
0.925 0.080 1 160128667 missense variant A/G snv 2