Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs13387042
LOC105373874 ; LOC101928278
0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs121909222
PTEN
0.742 0.240 10 87933127 missense variant A/G snv 13
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs6218
LINC02456 ; HELLPAR ; IGF1
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs172378
C1QA
0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs121917887
NME1-NME2 ; NME1
0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 10
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs1049074086
CTSD
0.925 0.120 11 1759567 missense variant A/G snv 7.0E-06 9
rs11662595
HRH4
0.882 0.120 18 24477006 missense variant A/G snv 8.6E-02 7.6E-02 7
rs1536309
MIR146B
0.851 0.160 10 102435445 upstream gene variant A/G snv 0.32 7
rs759478535
ERBB2
0.851 0.080 17 39708351 missense variant A/G snv 6.8E-05 4.2E-05 6
rs16940
BRCA1
0.882 0.080 17 43093220 synonymous variant A/G snv 0.35 0.29 5
rs1284410244
VEGFA
0.925 0.040 6 43778482 missense variant A/G snv 7.0E-06 4
rs147574894
NFKB1 ; LOC105377347
0.925 0.080 4 102600911 missense variant A/G snv 9.6E-05 3.9E-04 4
rs79036859
DAAM1
0.925 0.080 14 59369257 3 prime UTR variant A/G snv 3
rs899706404
SDHD ; TIMM8B
0.925 0.040 11 112087944 missense variant A/G snv 3
rs1156560901
CDK15
2 201880120 missense variant A/G snv 1.4E-05 2
rs1347591
NUP93
1.000 0.080 16 56834788 intron variant A/G snv 0.47 0.47 2
rs3804329
ATG5
1.000 0.080 6 106238552 intron variant A/G snv 0.15 2
rs723526
EGFR
1.000 7 55067126 intron variant A/G snv 0.86 2