Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs981042
CDKAL1
0.925 0.080 6 20535303 intron variant G/T snv 0.10 2
rs9808759
PCNT
1.000 0.080 21 46360308 intron variant T/A;C;G snv 1
rs9807667 1.000 0.080 18 71174376 intron variant G/A snv 0.14 1
rs9790517
TET2
0.925 0.080 4 105163621 intron variant C/T snv 0.20 2
rs975263
MACC1
0.827 0.120 7 20158817 stop gained G/A;T snv 0.34 7
rs974334
GPX6
0.925 0.080 6 28506441 intron variant C/G snv 0.26 0.29 2
rs9712235 1.000 0.080 2 67654625 intron variant G/A snv 0.68 1
rs970821
ANXA13 ; LOC105375739
1.000 0.080 8 123726378 intron variant C/T snv 0.36 1
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
rs9675999 1.000 0.080 18 23047728 intergenic variant G/A snv 0.48 1
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
rs9619765 1.000 0.080 22 38798063 upstream gene variant C/T snv 2.4E-02 1
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
rs9460578
CDKAL1
1.000 0.080 6 20923044 intron variant T/A snv 0.25 1