Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9823506
ABI3BP
1.000 0.080 3 100757869 intron variant C/T snv 4.3E-02 1
rs74180212 0.925 0.080 2 102181785 intron variant T/C;G snv 2
rs78545931 0.925 0.080 2 102265892 intergenic variant A/G snv 0.16 2
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs10208293
IL1RL1 ; IL18R1
0.882 0.160 2 102349850 intron variant G/A snv 0.33 2
rs1861245
IL18R1 ; IL1RL1
0.925 0.080 2 102350446 intron variant C/T snv 2
rs4988958
IL1RL1 ; IL18R1
1.000 0.080 2 102351825 synonymous variant T/C snv 0.34 0.46 1
rs71421264
TRAF3
1.000 0.080 14 102777733 intron variant C/A;G;T snv 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs201541519 1.000 0.080 14 105694756 intergenic variant AAGA/- delins 1.2E-02 2
rs6967330
CDHR3
0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 1
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs2052690
MRVI1
0.925 0.080 11 10642486 intron variant G/T snv 0.22 2
rs7734635 0.925 0.080 5 110823145 intergenic variant A/G snv 0.30 3
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs35032408
CLEC16A
0.925 0.080 16 11121567 intron variant T/C;G snv 2
rs12935657
CLEC16A
0.925 0.080 16 11125184 intron variant G/A snv 0.18 2
rs56317450
PHF14
1.000 0.080 7 11137720 intron variant G/A snv 0.18 1
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs143326447
MIR4435-2HG ; SOCAR
0.925 0.080 2 111511155 intron variant T/C snv 0.11 4
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs59289606
KIAA1958
1.000 0.080 9 112563085 intron variant C/A snv 0.16 1
rs892225
SBNO2
0.925 0.080 19 1152657 intron variant A/G snv 0.39 2
rs4807630
LOC102725180 ; SBNO2
1.000 0.080 19 1170446 intron variant C/T snv 0.26 1