Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs6498486
ERCC4
0.776 0.200 16 13919809 upstream gene variant A/C snv 0.27 8
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs115797771
KLF5
0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs1990172
MACC1
0.827 0.120 7 20164512 intron variant A/C snv 0.27 6
rs1625649
MGMT
0.882 0.080 10 129466667 upstream gene variant A/C snv 0.61 3
rs8003379
MTHFD1
0.882 0.160 14 64406881 intron variant A/C snv 0.23 3
rs121909242
PPARG
0.925 0.080 3 12416825 missense variant A/C snv 2
rs9858822
PPARG
0.925 0.080 3 12369739 intron variant A/C snv 0.11 2
rs12695175
CD47
1.000 0.080 3 108057799 intron variant A/C snv 0.12 1
rs1414714315
EPHA3
1.000 0.080 3 89413239 missense variant A/C snv 8.0E-06 1
rs180177033
BRAF
1.000 0.080 7 140781620 missense variant A/C snv 1
rs3742106
ABCC4
1.000 0.080 13 95021537 3 prime UTR variant A/C snv 0.41 0.37 1
rs4650708
PLA2G4A
1.000 0.080 1 186940985 intron variant A/C snv 0.25 1
rs63750448
GRN
1.000 0.080 17 44351792 synonymous variant A/C snv 1.6E-05 7.0E-06 1
rs63751121
FBXO11 ; MSH6
1.000 0.080 2 47799840 missense variant A/C snv 1.6E-05 4.9E-05 1
rs7130173
C11orf53
1.000 0.080 11 111283347 intron variant A/C snv 0.70 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1057910
CYP2C9
0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 12