Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34767364
NBN
0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 20
rs799917
BRCA1
0.708 0.320 17 43092919 missense variant G/A;C;T snv 0.40; 1.6E-05 18
rs2682818
MIR618 ; LOC105369869 ; LIN7A
0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs603965
CCND1
0.732 0.440 11 69648142 splice region variant G/A snv 14
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 13
rs1207011218
CTLA4
0.742 0.440 2 203870794 synonymous variant C/T snv 12
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs13706
CDC6
0.776 0.200 17 40300899 missense variant G/A;C snv 0.15; 8.0E-06 11
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs1052576
CASP9
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs16941
BRCA1
0.827 0.240 17 43092418 missense variant T/C;G snv 0.35 7
rs2509049
H2AX
0.827 0.160 11 119095811 upstream gene variant C/A;T snv 6
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 6
rs113686495
CASP8
0.925 0.160 2 201258757 intron variant ATTCTGTC/- delins 4
rs9610
IL10RA ; SMIM35
0.882 0.240 11 118001371 3 prime UTR variant G/A;T snv 0.51 4
rs147603016
FGFR4
0.925 0.160 5 177093286 synonymous variant G/A;C snv 1.5E-04; 8.2E-06 3
rs4901706
TMEM260
1.000 0.120 14 56647667 3 prime UTR variant G/A;C;T snv 3
rs6467
CYP21A2
0.925 0.320 6 32039081 missense variant C/A;G;T snv 0.64; 2.3E-03 3
rs10008492 1.000 0.120 4 38764099 intergenic variant C/G;T snv 2
rs121908689
RAD54L ; LRRC41
0.925 0.120 1 46272758 missense variant T/A snv 2
rs1801181
CBS
0.925 0.160 21 43060506 synonymous variant G/A snv 0.33 2
rs234706
CBS
0.925 0.160 21 43065240 synonymous variant G/A snv 0.27 2
rs3813729
C1RL ; C1R
0.925 0.120 12 7089608 missense variant C/G;T snv 2
rs606231364
FAS
0.925 0.160 10 89003071 missense variant G/A snv 2
rs758837678
NBN ; DECR1
0.925 0.120 8 90001503 missense variant C/T snv 2