Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1060915
BRCA1
1.000 0.080 17 43082453 synonymous variant A/G snv 0.35 0.30 1
rs1064795860
TP53
1.000 0.080 17 7675155 missense variant G/A snv 1
rs11075884 1.000 0.080 16 71321332 intergenic variant A/C;G snv 1
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 19
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1131691036
TP53
0.851 0.080 17 7675207 frameshift variant GCA/CC delins 8
rs113211432
BARD1
0.882 0.080 2 214767532 frameshift variant -/TG delins 3
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs1186364060
HFM1
1.000 0.080 1 91353084 missense variant C/T snv 1
rs121917739
RAD51
0.882 0.080 15 40718818 missense variant G/A snv 3.7E-04 1.7E-03 4
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs12516
BRCA1
0.851 0.160 17 43044391 3 prime UTR variant G/A snv 0.34 0.31 4
rs13010627
CASP10
0.807 0.280 2 201209375 missense variant G/A snv 4.2E-02 4.3E-02 10
rs1302297709
RAD51C
0.882 0.080 17 58703319 missense variant A/G snv 3
rs13387042
LOC105373874 ; LOC101928278
0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs1351211430
ERCC2
0.851 0.120 19 45369118 synonymous variant G/A;C snv 8.0E-06 4
rs140510218
CTCF
1.000 0.080 16 67621458 synonymous variant A/G snv 1.2E-05 7.0E-06 1