Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs2233678
PIN1 ; LOC100996288
0.732 0.360 19 9834503 non coding transcript exon variant G/A;C snv 14
rs1625895
TP53
0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs2228480
ESR1
0.724 0.360 6 152098960 synonymous variant G/A snv 0.19 0.18 16
rs2233682
PIN1
0.827 0.240 19 9838476 synonymous variant G/A snv 3.7E-02 6.3E-02 5
rs1351211430
ERCC2
0.851 0.120 19 45369118 synonymous variant G/A;C snv 8.0E-06 4
rs2272125
FANCD2 ; FANCD2OS
1.000 0.080 3 10096385 synonymous variant T/G snv 0.18 0.25 1
rs4986938
ESR2
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs7759
DPAGT1 ; H2AX
0.882 0.080 11 119096581 3 prime UTR variant A/G snv 0.30 3
rs1059394
TYMS ; ENOSF1
0.925 0.080 18 672792 3 prime UTR variant C/T snv 0.40 2
rs2790
TYMS ; ENOSF1
0.925 0.160 18 673086 3 prime UTR variant A/G;T snv 0.22 2
rs7350
H2AX
1.000 0.080 11 119094338 3 prime UTR variant G/A snv 0.30 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs2233679
PIN1 ; LOC100996288
0.763 0.360 19 9834678 splice region variant C/T snv 0.59 11
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs968728714
VDR
1.000 0.080 12 47904629 start lost A/G;T snv 1.5E-05; 7.4E-06 1