Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267606670
ATP1A3
0.790 0.320 19 41968837 missense variant C/A;T snv 19
rs606231435
ATP1A3
0.827 0.240 19 41970539 missense variant C/T snv 18
rs80356537
ATP1A3
0.752 0.320 19 41970405 missense variant C/A;G;T snv 17
rs387907281
ATP1A3
0.752 0.280 19 41970284 missense variant C/T snv 13
rs1064797245
ATP1A3
0.776 0.280 19 41970540 missense variant G/A snv 12
rs398122887
ATP1A3
0.790 0.280 19 41967744 missense variant C/G;T snv 8
rs557052809
ATP1A3
0.827 0.160 19 41975629 missense variant C/A;T snv 5
rs587777771
ATP1A3
0.851 0.240 19 41970275 missense variant C/T snv 4
rs387907282
ATP1A3
0.925 0.040 19 41970296 missense variant A/G snv 2
rs549006436
ATP1A3
0.925 0.040 19 41970389 missense variant A/C;T snv 2
rs606231442
ATP1A3
0.925 0.040 19 41969523 missense variant C/T snv 2
rs80356532
ATP1A3
0.925 0.040 19 41985090 missense variant A/G;T snv 2
rs80356534
ATP1A3
0.925 0.040 19 41978041 missense variant G/A snv 2
rs1555859571
ATP1A3
1.000 0.040 19 41970398 missense variant C/T snv 1
rs1568853466
ATP1A3
1.000 0.040 19 41969446 missense variant C/G snv 1
rs397515382
ATP1A3
1.000 0.040 19 41966938 inframe insertion -/TAG delins 1
rs397515577
ATP1A3
1.000 0.040 19 41976459 missense variant G/A snv 1
rs397515578
ATP1A3
1.000 0.040 19 41984930 inframe deletion CAG/- delins 1
rs573535377
ATP1A3
1.000 0.040 19 41981991 missense variant G/T snv 1
rs606231448
ATP1A3
1.000 0.040 19 41981956 missense variant A/G snv 1
rs606231449
ATP1A3
1.000 0.040 19 41981774 missense variant A/G snv 1
rs80356533
ATP1A3
1.000 0.040 19 41985082 missense variant C/T snv 1
rs80356535
ATP1A3
1.000 0.040 19 41970533 missense variant A/C snv 1
rs80356536
ATP1A3
1.000 0.040 19 41970468 missense variant A/G snv 1
rs869320661
ATP1A3
1.000 0.040 19 41984965 missense variant C/T snv 1