Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs2078087
NMNAT2
1 183389270 intron variant C/T snv 0.16 4
rs41307935
ZDHHC18
1.000 0.120 1 26854576 3 prime UTR variant C/T snv 6.1E-02 3
rs4949718
ST6GALNAC3
1 76433779 intron variant T/A;C snv 3
rs637868
PHGDH
1.000 0.120 1 119714487 splice region variant T/C snv 0.56 3
rs6684897 1.000 0.120 1 238128048 intergenic variant C/G snv 0.83 3
rs9436480
CDCP2
1 54151583 intron variant A/G snv 8.9E-02 2
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs16840760 2 204118831 intergenic variant T/C snv 3.6E-02 4
rs13395911
EFHD1
2 232655544 intron variant A/T snv 0.59 3
rs144104656 1.000 0.120 2 118661291 regulatory region variant A/G snv 1.1E-03 3
rs149940960
GREB1
1.000 0.120 2 11641492 3 prime UTR variant T/C snv 1.0E-02 3
rs206833 1.000 0.040 2 31485750 intergenic variant G/A snv 0.17 3
rs2241339
ABCB11
2 169013785 intron variant C/A;T snv 3
rs11124554
STRN
2 36922355 intron variant T/A;C snv 2
rs17801127
MMADHC-DT
2 149707970 intron variant C/T snv 8.6E-02 2
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs13077101
RABL3
3 120706484 intron variant T/C snv 4
rs892295
CHL1
3 355870 intron variant A/G snv 0.87 4
rs6550253
LINC01811
1.000 0.120 3 34149739 intron variant G/A snv 0.12 3
rs62269283
TM4SF4
3 149494481 intron variant G/A snv 1.9E-02 2
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs4835265
ZNF827
4 145900258 intron variant C/A snv 0.15 6
rs10001545 4 87254878 intergenic variant C/A;T snv 3
rs12500824
SHROOM3
1.000 0.040 4 76495474 intron variant A/G;T snv 3