Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4775936
MIR4713HG ; CYP19A1
0.790 0.200 15 51243825 intron variant C/T snv 0.36 7
rs4851527
IL1R2
0.790 0.160 2 102005914 intron variant A/G snv 0.63 7
rs3218896
IL1R2
0.807 0.160 2 102015190 intron variant T/C;G snv 6
rs1870050
GLDN
0.827 0.160 15 51344354 intron variant A/C snv 6.0E-02 5
rs10512263
TGFBR1
0.851 0.120 9 99123789 intron variant T/C snv 6.5E-02 4
rs117039649
MDM2
0.925 0.080 12 68808776 intron variant G/C snv 2.3E-02 4
rs1694964
LINC02025
0.925 0.080 3 84885341 intron variant G/T snv 4
rs28566535
CYP19A1
0.851 0.120 15 51308944 intron variant A/C;G;T snv 4
rs6478974
TGFBR1
0.851 0.120 9 99112121 intron variant A/G;T snv 4
rs749292
CYP19A1 ; MIR4713HG
0.851 0.160 15 51266534 intron variant G/A snv 0.44 4
rs8135424
CHEK2
0.925 0.080 22 28689804 intron variant G/A snv 0.14 4
rs1065779
CYP19A1 ; MIR4713HG
0.882 0.120 15 51212614 intron variant A/C;T snv 0.43 3
rs1204038
AR
0.882 0.160 X 67568383 intron variant G/A snv 0.36 3
rs12112075
OGDH
0.925 0.080 7 44609201 intron variant G/A snv 1.8E-02 3
rs12934561
IL32
0.882 0.080 16 3068864 intron variant T/C snv 0.57 3
rs2453839
IGFBP3
0.925 0.080 7 45913974 intron variant T/C snv 0.26 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
rs10502289
ENOSF1
0.925 0.080 18 676789 intron variant A/T snv 0.15 2
rs10733710
TGFBR1
0.925 0.080 9 99145142 intron variant G/A snv 0.21 2
rs11196445
CASP7
0.925 0.080 10 113710131 intron variant G/A snv 0.11 2
rs2298581
ENOSF1
0.925 0.080 18 677931 intron variant C/G snv 0.22 2
rs2298583
ENOSF1
0.925 0.080 18 677302 intron variant G/A snv 0.34 0.34 2
rs2494737
AKT1
0.925 0.080 14 104779988 intron variant T/A snv 0.40 2
rs2517951
ERBB2
0.925 0.080 17 39696844 intron variant C/T snv 0.52 2