Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000283
HSD11B1 ; HSD11B1-AS1
0.925 0.080 1 209721316 intron variant G/A snv 0.18 2
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10011540
UCP1
1.000 0.080 4 140568842 5 prime UTR variant T/G snv 0.10 1
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10011838 1.000 0.080 4 152599127 intergenic variant G/A snv 0.42 3
rs10012946
WFS1
1.000 0.080 4 6291623 intron variant T/C snv 0.63 1
rs1002630
CHN2
0.925 0.160 7 29388454 intron variant G/A snv 0.16 2
rs10034465
LINC02484
1.000 0.080 4 34193882 intron variant G/A snv 9.1E-02 2
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs10077431
YTHDC2
1.000 0.080 5 113591989 splice region variant C/A snv 0.15 0.16 1
rs10087241
PURG
1.000 0.080 8 31006206 intron variant G/A snv 0.56 1
rs1009358
LINC02576 ; LOC107984063 ; LINC02245
1.000 0.080 2 65049318 intron variant T/C snv 0.40 2
rs10100265
PINX1
1.000 0.080 8 10775649 intron variant A/C snv 0.60 1
rs10114341
LOC107987099
1.000 0.080 9 94156900 non coding transcript exon variant T/C snv 0.42 1
rs1011754
UBE2E2
1.000 0.080 3 23499566 intron variant A/G snv 4.2E-02 2.8E-02 1
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 6
rs10169613
MIR4435-2HG
1.000 0.080 2 111177400 intron variant C/T snv 0.42 1
rs1017568
GLIS3
1.000 0.080 9 3948365 intron variant T/C;G snv 1
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs10189773
ARHGAP15
1.000 0.080 2 143138931 intron variant A/G snv 0.20 1
rs10190052 1.000 0.080 2 646674 intergenic variant T/C snv 0.82 1
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs10203174
THADA
1.000 0.080 2 43462891 intron variant C/T snv 0.17 1
rs1020731
RBMS1
1.000 0.080 2 160287544 intron variant G/A snv 0.69 2