Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs969485
ARNTL
0.925 0.080 11 13381496 intron variant G/A snv 0.65 2
rs9693444 0.925 0.080 8 29652100 intergenic variant A/C snv 0.66 2
rs967624732
BRCA1
0.925 0.080 17 43097269 missense variant T/C snv 2
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs963918
RAD51B
0.827 0.120 14 68595397 3 prime UTR variant C/T snv 0.64 5
rs963917
RAD51B
0.827 0.120 14 68595606 3 prime UTR variant G/A snv 0.26 5
rs9620817
CHEK2
0.851 0.120 22 28712568 intron variant A/T snv 8.4E-02 4
rs9609643
SYN3 ; TIMP3
0.925 0.080 22 32855072 intron variant G/A snv 6.0E-02 2
rs9561778
ABCC4
0.851 0.120 13 95061461 intron variant G/A;T snv 4
rs9533156
TNFSF11
0.807 0.280 13 42573535 intron variant T/C snv 0.47 8
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs9485372
TAB2
0.807 0.120 6 149287738 intron variant G/A snv 0.20 6
rs9485370
TAB2
0.925 0.080 6 149285665 intron variant G/A;T snv 2
rs9479118
ESR1
0.925 0.080 6 151797989 intron variant T/C snv 1.6E-02 2
rs945453
ESRRG
0.925 0.080 1 216519327 synonymous variant C/A;T snv 0.51 2
rs942755287
ARHGAP24
0.925 0.080 4 85972113 missense variant C/T snv 7.0E-06 2
rs941764
CCDC88C
0.925 0.080 14 91374725 intron variant A/G snv 0.46 2
rs941759532
ERCC4
0.763 0.240 16 13932175 missense variant C/G snv 11
rs941735789
PANX2
1.000 0.080 22 50177152 missense variant C/T snv 1
rs9397435 0.925 0.080 6 151630085 regulatory region variant A/G snv 7.6E-02 2
rs9393597
RIPOR2
0.925 0.080 6 24972880 intron variant A/G snv 0.15 2
rs9383938
ESR1
0.827 0.160 6 151666222 intron variant G/T snv 0.11 5
rs9383935
LOC107986528 ; CCDC170
0.925 0.080 6 151618713 3 prime UTR variant C/T snv 7.0E-02 2
rs9383590 0.925 0.080 6 151632630 intergenic variant T/C snv 6.0E-02 2
rs9380142
HLA-G
0.925 0.080 6 29831017 3 prime UTR variant A/G snv 0.27 2