Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 7
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50 7
rs3020314
ESR1
0.790 0.280 6 151949537 intron variant C/G;T snv 7
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
rs11263763
HNF1B
0.882 0.200 17 37743574 intron variant A/G snv 0.43 6
rs13429458
THADA
0.827 0.200 2 43411699 intron variant A/C snv 0.14 6
rs3218896
IL1R2
0.807 0.160 2 102015190 intron variant T/C;G snv 6
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv 6
rs11658063
HNF1B
0.851 0.120 17 37743881 intron variant G/C;T snv 5
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
rs2479106
DENND1A
0.851 0.120 9 123762933 intron variant A/G snv 0.44 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
rs10431924
CDH1
0.882 0.120 16 68805399 intron variant T/C snv 0.45 3
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
rs12185157
CDH1
0.882 0.120 16 68750684 intron variant G/A;C;T snv 3
rs12934561
IL32
0.882 0.080 16 3068864 intron variant T/C snv 0.57 3