Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9967983
SOD1
0.925 0.080 21 31665169 intron variant A/T snv 0.47 2
rs996427
PLCL1
1.000 0.080 2 197820885 intron variant G/A snv 0.20 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9915936
AXIN2
0.827 0.120 17 65537671 synonymous variant T/C snv 0.90 0.90 5
rs9900242
CASC17
0.925 0.080 17 71139490 intron variant G/A snv 0.32 2
rs9889335
CASC17
1.000 0.080 17 71119005 intron variant T/G snv 0.59 1
rs9852810
MLH1
0.882 0.080 3 37027478 intron variant G/A snv 0.35 3
rs985081 1.000 0.080 X 149456568 intergenic variant T/C snv 0.14 1
rs980171
LOC105375751 ; PCAT1
0.925 0.080 8 127042277 intron variant A/G snv 0.45 2
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs968098233
AR
0.882 0.200 X 67546162 missense variant T/C snv 3
rs9666607
CD44
0.925 0.080 11 35204608 missense variant A/G;T snv 0.74 2
rs9658655
CHGA
0.925 0.080 14 92931686 missense variant G/C snv 0.13 0.12 2
rs9656816 1.000 0.080 8 127522409 intergenic variant G/A snv 0.94 1
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9623117
TNRC6B
0.851 0.200 22 40056115 intron variant T/C snv 0.38 4
rs9608380
CRYBB2
0.925 0.080 22 25226475 intron variant C/T snv 0.12 2
rs9600079 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 5
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs946993012
NOS1
0.925 0.080 12 117331056 missense variant A/G snv 4.0E-06 1.4E-05 2
rs9393682
H1-2
0.925 0.080 6 26056822 upstream gene variant C/T snv 9.8E-02 2
rs9388766
L3MBTL3
0.925 0.080 6 130033710 intron variant T/C snv 0.65 3
rs9375701
L3MBTL3
0.827 0.160 6 130062912 intron variant C/T snv 0.53 6
rs937475913
PRKDC
0.790 0.120 8 47936435 missense variant T/C snv 4.0E-06 7