Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 11
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs20576
TNFRSF10A
0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs6869366
XRCC4 ; TMEM167A
0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs35866072
MMP8
0.716 0.360 11 102713373 missense variant T/G snv 6.0E-02 9.8E-02 17
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs10511729
LOC101929563
0.742 0.240 9 23557229 intron variant T/G snv 0.35 11
rs4957014
AHRR ; PDCD6
0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs2602141
TP53BP1
0.790 0.120 15 43432448 missense variant T/G snv 0.36 0.47 9
rs45446698
CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 9
rs2070584
TIMP1 ; MIR4769 ; SYN1
0.790 0.200 X 47587120 intron variant T/G snv 0.44 8
rs2240688
FGFBP2 ; PROM1
0.790 0.160 4 15968726 3 prime UTR variant T/G snv 0.22 7
rs6759892
UGT1A6 ; UGT1A9 ; UGT1A7 ; UGT1A8 ; UGT1A10
0.851 0.160 2 233693023 missense variant T/G snv 0.39 0.39 7
rs7775397
TSBP1-AS1 ; TSBP1
0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 7
rs1063054
NBN ; OSGIN2
0.807 0.160 8 89934373 3 prime UTR variant T/G snv 0.32 6
rs2854509
XRCC1
0.807 0.160 19 43570445 intron variant T/G snv 0.80 6
rs11778573
CCN4
0.851 0.080 8 133216687 intron variant T/G snv 0.59 4
rs12674822
MCPH1 ; ANGPT2
0.851 0.200 8 6531695 intron variant T/G snv 0.49 4