Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9940874
MARF1
16 15634417 intron variant T/C snv 0.18 2
rs9937036 16 16636871 intron variant T/A;C;G snv 3
rs9601485 13 80901307 intron variant C/T snv 0.28 2
rs9436480
CDCP2
1 54151583 intron variant A/G snv 8.9E-02 2
rs892295
CHL1
3 355870 intron variant A/G snv 0.87 4
rs8182496 19 31643033 intergenic variant C/T snv 0.46 2
rs8108722 19 10236408 intergenic variant T/A;C snv 2
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs7803882 7 55869748 intergenic variant T/A;C snv 2
rs76861960 16 77565542 intergenic variant T/C snv 1.3E-02 2
rs754465
DLG5
10 77920756 intron variant C/A snv 0.52 2
rs74913549
PANX1
11 94180526 intron variant T/A;C snv 3
rs74709575
LINC02334
1.000 0.120 13 38041119 intron variant A/C snv 3.1E-03 3
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs738408
PNPLA3
0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22 10
rs73186036
N6AMT1
21 28754160 regulatory region variant A/G snv 0.20 2
rs72772090
CAST
1.000 0.120 5 96700607 intron variant G/A;C snv 3
rs7122144 11 129520077 intergenic variant T/C snv 0.16 2
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs6684897 1.000 0.120 1 238128048 intergenic variant C/G snv 0.83 3
rs6550253
LINC01811
1.000 0.120 3 34149739 intron variant G/A snv 0.12 3
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs637868
PHGDH
1.000 0.120 1 119714487 splice region variant T/C snv 0.56 3
rs62269283
TM4SF4
3 149494481 intron variant G/A snv 1.9E-02 2
rs4979372
AKNA
9 114377802 intron variant T/C;G snv 2