Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143046984
LOC105370557 ; PCNX1
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02 9
rs80359601
BRCA2
0.807 0.360 13 32340890 frameshift variant -/A;NNNNNNNN ins 4.1E-06 8
rs202110856
ERAP1
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05 9
rs377429877
STARD13
0.776 0.080 13 33518027 intron variant -/TAA delins 6.0E-02 10
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs6058093
PIGU
0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs9924886
CDH3
0.776 0.080 16 68710036 intron variant A/C snv 0.25 10
rs10911251
LAMC1
0.790 0.080 1 183112059 intron variant A/C snv 0.37 9
rs16973225
LOC102724001
0.790 0.080 15 81937658 intron variant A/C snv 7.4E-02 9
rs2184857
LOC105373224
0.790 0.080 1 239918447 upstream gene variant A/C snv 0.45 9
rs6720296
LINC01121
0.790 0.080 2 45181130 intron variant A/C snv 0.52 9
rs73975588
NXN
0.790 0.080 17 913501 intron variant A/C snv 9.9E-02 9
rs769240800
PALB2
0.925 0.120 16 23638116 stop gained A/C snv 8.0E-06 3
rs764355898
NRK
1.000 0.080 X 105923145 missense variant A/C snv 7.9E-05 1.9E-05 1
rs11150038
CLEC3A
0.790 0.080 16 78042662 intron variant A/C;G snv 10
rs17102823 0.776 0.080 14 34894698 intergenic variant A/C;G snv 10
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs35107139
BMP4
0.776 0.080 14 53952388 intron variant A/C;G;T snv 11
rs4768903
DIP2B
0.790 0.080 12 50651666 intron variant A/C;G;T snv 9
rs2250430
PLEKHG6
0.776 0.080 12 6312008 intron variant A/C;T snv 10
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12 9
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs2735940
TERT
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24