Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs997476 0.882 0.080 4 102620848 downstream gene variant G/T snv 4.3E-02 3
rs9929218
CDH1
0.732 0.160 16 68787043 intron variant G/A snv 0.28 16
rs9904341
BIRC5
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs9869263
LOC107986170 ; CLDN1
0.925 0.080 3 190312891 synonymous variant A/C;G;T snv 8.0E-06; 0.83; 4.0E-06 3
rs975263
MACC1
0.827 0.120 7 20158817 stop gained G/A;T snv 0.34 7
rs9694958
IKBKB ; LOC105379395
0.925 0.080 8 42298528 intron variant A/G snv 0.26 2
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 15
rs9365723
SYNJ2
0.827 0.080 6 158014540 intron variant A/C;G snv 0.56 5
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs910532454
CXCR4
0.882 0.080 2 136115453 missense variant C/A;T snv 4.0E-06 4
rs909797662
EGFR
0.790 0.120 7 55191837 missense variant G/A snv 8
rs8905
PRKAR1A ; FAM20A
0.925 0.080 17 68531661 3 prime UTR variant T/A;G snv 2
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs876658198
MLH1
0.925 0.080 3 37028855 missense variant G/A snv 2
rs8191754
IGF2R
0.925 0.080 6 160027292 missense variant C/G snv 0.13 0.13 2
rs8176318
BRCA1
0.807 0.120 17 43045257 3 prime UTR variant C/A snv 0.34 0.29 6
rs8124792
CYP24A1
0.827 0.120 20 54150268 downstream gene variant G/A snv 7.8E-02 6
rs8086
ACSL1
0.925 0.080 4 184756267 3 prime UTR variant C/T snv 0.24 2
rs8073069
BIRC5
0.807 0.200 17 78213692 upstream gene variant G/C snv 0.33 7
rs8039880
MAP2K1
0.925 0.080 15 66468004 intron variant A/G snv 0.21 2
rs7987649
FLT1
0.925 0.080 13 28320278 intron variant A/G snv 0.35 4
rs7911488
MIR1307 ; ATP5MD
0.882 0.080 10 103394332 5 prime UTR variant A/G snv 0.34 0.26 3
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93