Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13347
CD44
0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 12
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs236918
PCSK7
0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs1553553086
FARSB
0.827 0.280 2 222623699 missense variant C/T snv 9
rs1041740
SOD1
0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 8
rs41295061 0.790 0.360 10 6072697 upstream gene variant C/A snv 6.1E-02 8
rs4646437
CYP3A4
0.827 0.200 7 99767460 intron variant G/A snv 0.30 8
rs910049
TSBP1-AS1 ; TSBP1
0.776 0.400 6 32347950 intron variant T/C snv 0.76 8
rs10053538
HAVCR2
0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs11003123
MBL2
0.827 0.200 10 52771774 upstream gene variant G/A snv 0.30 6
rs12304647
MIR196A2 ; HOXC6
0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 5
rs1054690270
LOC101928953 ; GPT
0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs10932029
ICOS ; LOC101927840
0.827 0.200 2 203937045 intron variant T/A;C snv 5
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs1396171148
FARSB
0.851 0.200 2 222613892 missense variant T/G snv 5