Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11571818
BRCA2
0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs11844632
RAD51B
0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv 17
rs481519
NEK10
0.708 0.280 3 27285723 intron variant C/A;T snv 17
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02 17
rs73110464
KRT8
0.708 0.280 12 52918828 intron variant C/T snv 0.12 17
rs7725218
TERT
0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs2242652
TERT
0.724 0.400 5 1279913 intron variant G/A snv 0.18 16
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16
rs7003908
PRKDC
0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv 16
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs28360317
XRCC4
0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 14
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41 12