Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9933638
TOX3
0.882 0.080 16 52505685 intron variant A/G snv 0.41 3
rs9915936
AXIN2
0.827 0.120 17 65537671 synonymous variant T/C snv 0.90 0.90 5
rs9912300
ACLY
0.827 0.120 17 41869011 intron variant G/A;C;T snv 4.2E-06; 0.78 5
rs9895829
TP53
0.807 0.080 17 7675361 5 prime UTR variant A/G snv 7.4E-02 6
rs974494
LOC105372974 ; SEZ6L
1.000 0.080 22 26254399 intron variant C/G;T snv 1
rs974404
AP4B1-AS1 ; PTPN22
1.000 0.080 1 113839403 intron variant G/A;T snv 1
rs973682124
PPP2R1B
1.000 0.080 11 111743419 missense variant T/C snv 4.0E-06 7.0E-06 1
rs969129
LOC105374724 ; IL7R
0.851 0.200 5 35861166 intron variant T/A;G snv 4
rs968643096
RB1
1.000 0.080 13 48453041 missense variant C/T snv 1
rs967591
CD3EAP ; PPP1R13L
0.851 0.080 19 45406676 5 prime UTR variant G/A;C;T snv 0.22; 6.7E-06 4
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs9625933
HORMAD2
1.000 0.080 22 30159227 intron variant G/A snv 0.21 1
rs9625919
HORMAD2
1.000 0.080 22 30104969 intron variant G/T snv 0.21 1
rs9625874
MTMR3
1.000 0.080 22 29892636 intron variant A/G snv 0.21 1
rs9620953
HORMAD2
1.000 0.080 22 30150256 intron variant C/T snv 0.20 1
rs9614162
LOC105372988
1.000 0.080 22 30208113 upstream gene variant G/A snv 0.30 1
rs9614159
LOC105372988 ; HORMAD2
0.882 0.160 22 30205254 intron variant G/A snv 0.30 3
rs9614158
LOC105372988 ; HORMAD2
1.000 0.080 22 30201891 intron variant A/G snv 0.22 1
rs9614157
LOC105372988 ; HORMAD2
1.000 0.080 22 30201821 intron variant A/G snv 0.26 1
rs9554314
FLT1
0.851 0.080 13 28301652 3 prime UTR variant A/C snv 4
rs9535826
ATP7B
0.851 0.080 13 51991990 intron variant T/C;G snv 4
rs950776
CHRNB4
1.000 0.080 15 78633676 intron variant T/C snv 0.26 3
rs9469031
PRRC2A
0.882 0.080 6 31628018 missense variant C/T snv 6.6E-03 5.9E-03 3
rs941759532
ERCC4
0.763 0.240 16 13932175 missense variant C/G snv 11
rs9387478
DCBLD1
0.851 0.080 6 117465017 intron variant C/A;T snv 4