Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10012
CYP1B1 ; CYP1B1-AS1
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 7
rs10046
MIR4713HG ; CYP19A1
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042838
PGR
0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 12
rs10431923
CDH1
0.925 0.120 16 68805360 intron variant G/T snv 0.44 2
rs10431924
CDH1
0.882 0.120 16 68805399 intron variant T/C snv 0.45 3
rs1045242
TNFAIP8
0.925 0.080 5 119393632 3 prime UTR variant A/G snv 0.32 3
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1048290
KEAP1
0.851 0.160 19 10489766 synonymous variant G/C snv 0.41 0.48 4
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs10502289
ENOSF1
0.925 0.080 18 676789 intron variant A/T snv 0.15 2
rs10512263
TGFBR1
0.851 0.120 9 99123789 intron variant T/C snv 6.5E-02 4
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1056827
CYP1B1 ; CYP1B1-AS1
0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 7
rs1057519945
POLE
0.776 0.200 12 132673703 missense variant C/A;T snv 12
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1059234
CDKN1A
0.790 0.120 6 36685820 3 prime UTR variant C/T snv 0.15 0.13 10
rs1063539
ADIPOQ ; ADIPOQ-AS1
0.827 0.360 3 186857603 3 prime UTR variant G/A;C snv 0.10 5
rs1065779
CYP19A1 ; MIR4713HG
0.882 0.120 15 51212614 intron variant A/C;T snv 0.43 3
rs10733710
TGFBR1
0.925 0.080 9 99145142 intron variant G/A snv 0.21 2