Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7796976
LOC101927609 ; AHR
0.925 0.040 7 17298806 5 prime UTR variant A/G snv 0.79 3
rs140135
ZMAT5 ; UQCR10
0.827 0.120 22 29767846 non coding transcript exon variant C/G snv 0.79 5
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs4372078
TNFSF15
1.000 0.040 9 114801407 intron variant T/G snv 0.78 1
rs6708413
IL18RAP
1.000 0.040 2 102446909 intron variant G/A snv 0.78 2
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 4
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs6740462
LOC105374780
1.000 0.040 2 65440138 intron variant C/A snv 0.78 2
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 4
rs832582
MAP3K1
0.925 0.080 5 56881916 missense variant G/A snv 0.76 0.78 2
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 3
rs6556411
LOC285626
0.827 0.120 5 159356215 intron variant G/T snv 0.77 5
rs941823
LINC00598
0.827 0.120 13 40439840 intron variant T/C snv 0.77 6
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5
rs4785220
NKD1
1.000 0.040 16 50593467 intron variant T/C snv 0.77 1
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 6
rs7313895
LRRK2
0.827 0.120 12 40350592 intron variant G/T snv 0.77 5
rs11209002
C1orf141
1.000 0.040 1 67124778 intron variant T/C snv 0.77 1
rs1520339
LOC105373703
1.000 0.040 2 155895409 regulatory region variant T/C snv 0.76 2
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 12
rs2451258
LOC112267968
0.807 0.160 6 159085568 intron variant C/T snv 0.75 6
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 7
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12