Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5031015
MIR4761 ; COMT
0.925 0.080 22 19963580 missense variant G/A snv 6.9E-04 2.5E-03 2
rs11224561
PGR
0.925 0.080 11 101034325 3 prime UTR variant C/A;T snv 2
rs471767
PGR
0.925 0.080 11 101034566 3 prime UTR variant G/A;C snv 2
rs2677764
PIK3CA
0.925 0.080 3 179206019 intron variant C/A;T snv 2
rs9838411
PIK3CA
0.925 0.080 3 179169899 intron variant G/A snv 0.25 2
rs758188449
SHBG
0.925 0.080 17 7632936 missense variant G/A;T snv 6.8E-05; 4.0E-06 2
rs1182154114
SULT1A1
0.925 0.080 16 28623160 missense variant G/C snv 2
rs10733710
TGFBR1
0.925 0.080 9 99145142 intron variant G/A snv 0.21 2
rs201768983
TNK2
0.925 0.080 3 195868640 missense variant C/T snv 1.2E-04 3.5E-05 2
rs4721745
TWIST1
0.925 0.080 7 19113889 3 prime UTR variant C/G snv 0.18 2
rs3731127
XPC
0.925 0.080 3 14158973 intron variant G/A snv 4.0E-02 2
rs1204038
AR
0.882 0.160 X 67568383 intron variant G/A snv 0.36 3
rs1451539938
CD82
0.925 0.080 11 44618361 missense variant A/G snv 4.1E-06 7.0E-06 3
rs1065779
CYP19A1 ; MIR4713HG
0.882 0.120 15 51212614 intron variant A/C;T snv 0.43 3
rs2453839
IGFBP3
0.925 0.080 7 45913974 intron variant T/C snv 0.26 3
rs12934561
IL32
0.882 0.080 16 3068864 intron variant T/C snv 0.57 3
rs1156807933
MAX ; LOC100506321
0.925 0.080 14 65093799 missense variant T/C snv 4.0E-06 3
rs12112075
OGDH
0.925 0.080 7 44609201 intron variant G/A snv 1.8E-02 3
rs2475335
PTPRD
0.882 0.080 9 10260263 intron variant C/A;T snv 3
rs4980524
STIP1
0.882 0.080 11 64191787 intron variant A/C;T snv 3
rs1045242
TNFAIP8
0.925 0.080 5 119393632 3 prime UTR variant A/G snv 0.32 3
rs1200003171
AKT1
0.882 0.120 14 104775122 missense variant C/A;T snv 8.0E-06 4
rs11196418
CASP7
0.925 0.080 10 113678707 upstream gene variant G/A snv 0.11 4
rs8135424
CHEK2
0.925 0.080 22 28689804 intron variant G/A snv 0.14 4
rs28566535
CYP19A1
0.851 0.120 15 51308944 intron variant A/C;G;T snv 4