Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1997179 1.000 0.080 4 122063478 intergenic variant T/C snv 0.21 1
rs2097282 1.000 0.080 3 46336534 intergenic variant C/T snv 0.68 1
rs2157453 1.000 0.080 1 172894808 intron variant G/A snv 0.31 1
rs2187670 1.000 0.080 3 46325463 intergenic variant T/C snv 0.81 1
rs4558075 1.000 0.080 10 6359663 intergenic variant C/A;G;T snv 1
rs4899260 1.000 0.080 14 68811487 intergenic variant C/T snv 0.28 1
rs4946111 1.000 0.080 6 115663255 intergenic variant T/A;G snv 1
rs4956400 1.000 0.080 4 141556189 intergenic variant T/C snv 0.75 1
rs62184863 1.000 0.080 2 203819074 intergenic variant G/C snv 6.2E-02 1
rs6762743 1.000 0.080 3 179294212 intergenic variant C/T snv 0.29 1
rs7104791 1.000 0.080 11 111326133 downstream gene variant T/A;C snv 1
rs77027760 1.000 0.080 6 137680924 intron variant G/A snv 0.15 1
rs859715 1.000 0.080 1 172790982 intron variant A/T snv 0.36 1
rs9391227 1.000 0.080 6 104710759 regulatory region variant T/A snv 0.56 1
rs971290 1.000 0.080 14 68805252 intergenic variant C/A;G;T snv 1
rs72653706
ABCC6
0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs8081319
ACACA ; C17orf78
1.000 0.080 17 37374139 intron variant A/G snv 6.8E-02 1
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs11123810
AFF3
0.925 0.200 2 100142823 intron variant T/C snv 0.37 2
rs7100025
ANKRD30A ; LINC00993
0.724 0.240 10 37303610 intron variant G/A snv 0.68 14
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs771541567
APOB
0.851 0.120 2 21029900 missense variant G/A;T snv 8.0E-06; 2.0E-05 4
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5