Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs849136
JAZF1
0.851 0.240 7 28135338 intron variant A/G snv 0.74 4
rs2274911
GPRC6A
0.851 0.160 6 116809541 missense variant G/A snv 0.72 0.74 6
rs1058205
KLK3
0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 3
rs2229113
IL10RA
0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs171866 0.925 0.080 6 115870638 intergenic variant G/A snv 0.73 2
rs2705897
CASP3
0.925 0.080 4 184631944 splice region variant T/G snv 0.64 0.73 4
rs1417939
STOX1
0.925 0.080 10 68874648 intron variant G/A snv 0.73 2
rs10749408 0.925 0.080 10 121208012 intergenic variant C/T snv 0.72 2
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs11781886
NKX3-1 ; LOC107986930
0.925 0.080 8 23682904 5 prime UTR variant C/T snv 0.72 0.72 2
rs10931777
ANKRD44-IT1 ; ANKRD44
1.000 0.080 2 197278867 intron variant C/T snv 0.72 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2394882
POU5F1 ; TCF19
0.882 0.080 6 31164872 splice region variant A/C snv 0.64 0.69 3
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs651164
SLC22A1
0.882 0.160 6 160160342 downstream gene variant A/G snv 0.69 3
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs4794758
HNF1B ; LOC105371754
0.925 0.080 17 37720433 intron variant T/C snv 0.66 2
rs7003908
PRKDC
0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs928554
ESR2
0.851 0.120 14 64227477 3 prime UTR variant C/T snv 0.66 6
rs2359612
VKORC1
0.851 0.120 16 31092475 intron variant A/G snv 0.66 7
rs1815009
IGF1R
0.925 0.080 15 98961442 3 prime UTR variant C/T snv 0.65 3
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60