Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1885119
TRPC4AP
1.000 0.080 20 35057846 intron variant T/C snv 0.58 3
rs2065108
MMP24-AS1-EDEM2 ; EDEM2
1.000 0.080 20 35119019 intron variant C/T snv 0.61 3
rs2632516
TSPOAP1-AS1 ; MIR142
1.000 0.080 17 58331728 non coding transcript exon variant G/A;C snv 0.51 3
rs41290120
NECTIN2
1.000 0.080 19 44879418 intron variant G/A;T snv 3
rs4605275 1.000 0.080 19 44835236 intergenic variant T/C snv 0.69 3
rs5963409
OTC
1.000 0.080 X 38351716 intron variant A/C;G snv 3
rs6087664
TRPC4AP
1.000 0.080 20 35038413 intron variant C/A;G;T snv 3
rs6088692
TRPC4AP
1.000 0.080 20 35050785 intron variant A/G snv 0.58 3
rs6088727
MMP24-AS1-EDEM2 ; EDEM2
1.000 0.080 20 35125836 intron variant G/A snv 0.51 3
rs6120816
TRPC4AP
1.000 0.080 20 35056555 intron variant G/A;C snv 3
rs6334
NTRK1
1.000 0.080 1 156876441 missense variant G/A;C;T snv 0.22; 4.0E-06 3
rs63750072
MAPT
1.000 0.080 17 45983493 missense variant A/G snv 4.0E-02 3.8E-02 3
rs75627662 1.000 0.080 19 44910319 non coding transcript exon variant C/T snv 0.17 3
rs759819 1.000 0.080 19 54304302 intron variant C/G;T snv 3
rs7935829
MS4A6A
1.000 0.080 11 60175342 intron variant A/G snv 0.33 3
rs10401176
BCL3
1.000 0.080 19 44750234 intron variant C/G;T snv 0.17 2
rs10426401
LOC107985305 ; PVR
1.000 0.080 19 44644419 intron variant T/G snv 0.32 2
rs1048699
PPP1R37 ; MARK4
1.000 0.080 19 45147128 3 prime UTR variant C/T snv 9.0E-02 2
rs1050565
BLMH
1.000 0.080 17 30249058 missense variant T/C snv 0.30 0.29 2
rs10792832 1.000 0.080 11 86156833 downstream gene variant A/G snv 0.70 2
rs10808026
EPHA1
1.000 0.080 7 143402040 intron variant C/A snv 0.19 2
rs11082498
EPG5
1.000 0.080 18 45922762 intron variant T/C snv 0.37 2
rs1114832
PPP1R37 ; MARK4
1.000 0.080 19 45132943 intron variant C/T snv 9.2E-02 2
rs11230201
MS4A4E ; MS4A4A
1.000 0.080 11 60229521 intron variant C/G;T snv 2
rs11244787
ADAM12
1.000 0.080 10 126046147 intron variant A/G snv 0.13 0.13 2