Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs523349
SRD5A2
0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs9282858
SRD5A2
0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 16
rs121907900
WT1
0.763 0.200 11 32392020 missense variant G/A snv 11
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 10
rs9332964
SRD5A2
0.763 0.240 2 31529325 missense variant C/T snv 4.7E-04 1.6E-04 10
rs2066479
HSD17B3
0.790 0.160 9 96235528 missense variant C/A;G;T snv 7.2E-02 7
rs1110061
NR5A1
0.807 0.200 9 124500523 missense variant C/A;G snv 4.3E-06; 0.10 7
rs121434250
SRD5A2
0.790 0.200 2 31529419 missense variant C/G;T snv 1.4E-04 1.5E-04 7
rs9332967
SRD5A2
0.790 0.200 2 31526224 missense variant C/T snv 2.3E-04 1.1E-04 7
rs944050
ESR2
0.827 0.280 14 64233327 splice region variant T/C snv 9.5E-02 7.9E-02 5
rs1037084691
WT1
0.827 0.160 11 32392031 missense variant C/G;T snv 5
rs554416372
WT1
0.827 0.160 11 32396397 missense variant C/A;G;T snv 2.0E-05; 8.0E-06; 9.6E-05 5
rs2069521 0.851 0.240 15 74746626 upstream gene variant G/A snv 4.9E-02 4
rs6785358 0.882 0.200 3 30602723 upstream gene variant G/A snv 0.84 4
rs765057534
CYP19A1 ; MIR4713HG
0.851 0.240 15 51222402 missense variant C/T snv 4.0E-06 4
rs121918508
FGFR2
0.851 0.360 10 121488035 missense variant C/T snv 4
rs1057517779
NR5A1
0.851 0.160 9 124493083 missense variant G/A snv 4
rs4919686
WBP1L ; CYP17A1 ; CYP17A1-AS1
0.851 0.200 10 102832492 3 prime UTR variant A/C snv 0.23 0.21 4
rs2278705 0.882 0.160 15 80402288 intron variant C/T snv 4.2E-02 3
rs1020397
ARNT2
0.882 0.160 15 80426396 intron variant G/C;T snv 3
rs5000770
ARNT2
0.882 0.160 15 80424141 intron variant G/A snv 0.27 3