Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6846071
BANK1
4 101481058 intron variant T/G snv 0.15 2
rs6951245
C7orf50
7 1018557 intron variant G/A snv 0.12 2
rs771767 1.000 0.080 3 102029794 regulatory region variant A/G snv 0.70 2
rs9284725
IL1R1
2 102128394 intron variant C/A;T snv 0.82 1
rs4141632
IL1R1
2 102140679 intron variant A/G;T snv 1
rs10745954
C12orf42
12 103089316 intron variant A/G snv 0.60 1
rs10778213
C12orf42
12 103101373 intron variant T/C snv 0.57 1
rs4764725
C12orf42
12 103118536 intron variant T/C snv 0.56 1
rs10778215
C12orf42
12 103143488 intron variant T/A;G snv 2
rs1529711
CARM1
1.000 0.080 19 10912758 intron variant C/T snv 0.13 4
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs10744775
BRAP
12 111658411 intron variant T/C snv 0.44 2
rs10255299
DOCK4
7 111887504 intron variant G/A snv 0.11 2
rs5744256
IL18
0.827 0.120 11 112152125 intron variant A/G snv 0.16 6
rs1834481
IL18
0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16 5
rs5744222
TEX12 ; LOC107987164
11 112166291 intron variant G/A;T snv 1
rs7131094
BCO2
11 112174194 intron variant C/T snv 0.17 1
rs10891343
BCO2
11 112209661 intron variant T/C snv 0.44 2
rs2250417
BCO2
1.000 0.080 11 112214593 intron variant T/C snv 0.44 5
rs2285810
HECTD4
12 112261736 non coding transcript exon variant T/C snv 0.45 2
rs6761276
IL1F10
2 113074735 missense variant T/C snv 0.56 0.57 2
rs6743376
IL1F10
2 113074756 missense variant C/A snv 0.69 0.69 2
rs13386602 2 113077243 downstream gene variant A/C snv 0.56 1
rs11678375 2 113078114 downstream gene variant T/C snv 0.56 1