Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10054504
PDZD2
1.000 0.120 5 32000377 intron variant T/A;C snv 1
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1010980331
FLCN ; MPRIP
0.925 0.120 17 17215072 missense variant T/C snv 2
rs10211665
EPAS1
1.000 0.120 2 46298957 intron variant T/C snv 0.58 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs10484683
SAMD5
1.000 0.120 6 147830941 intron variant A/G snv 0.18 1
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104893824
VHL
0.776 0.320 3 10142181 missense variant T/A;C snv 8
rs104893829
VHL
0.882 0.240 3 10142088 missense variant C/T snv 2.0E-04 3.8E-04 4
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1049380
ITPR2
0.827 0.120 12 26336611 3 prime UTR variant G/T snv 0.69 5
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057519913
MTOR
0.925 0.120 1 11157172 missense variant G/C snv 3
rs1057519914
MTOR
0.851 0.240 1 11157174 missense variant A/G snv 5
rs1057519915
MTOR
0.851 0.160 1 11109318 missense variant A/C snv 5
rs1057519916
MTOR
0.882 0.160 1 11109320 missense variant T/A snv 4
rs1057519917
MTOR
0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs1057519920
NFE2L2
0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 10
rs1057519929
PIK3CA
0.776 0.320 3 179199066 missense variant G/A snv 10
rs1057519932
PIK3CA
0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519949
RHEB
0.851 0.120 7 151490964 missense variant A/T snv 6
rs1057519950
RHEB
0.827 0.200 7 151490963 missense variant T/A;C snv 5
rs1057519960
SF3B2
0.827 0.280 11 66063413 missense variant A/G snv 7