Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs376674848 1.000 0.080 12 84220725 intron variant -/ATGTGT delins 1
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs80357929
BRCA1
0.851 0.200 17 43092663 frameshift variant A/- del 4
rs80359306
BRCA2
0.827 0.280 13 32333284 frameshift variant A/-;AA delins 6
rs587776701
MSH3
0.925 0.080 5 80675096 frameshift variant A/-;AA delins 2.1E-05 2
rs13429458
THADA
0.827 0.200 2 43411699 intron variant A/C snv 0.14 6
rs1870050
GLDN
0.827 0.160 15 51344354 intron variant A/C snv 6.0E-02 5
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs911162
AURKA ; CSTF1
1.000 0.080 20 56391393 intron variant A/C;G snv 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs28566535
CYP19A1
0.851 0.120 15 51308944 intron variant A/C;G;T snv 4
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs80357115
BRCA1
0.790 0.200 17 43092597 stop gained A/C;T snv 8
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv 7
rs1065779
CYP19A1 ; MIR4713HG
0.882 0.120 15 51212614 intron variant A/C;T snv 0.43 3
rs4980524
STIP1
0.882 0.080 11 64191787 intron variant A/C;T snv 3
rs10908278
HNF1B
0.925 0.160 17 37739961 intron variant A/C;T snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45