Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4978754
ELP1
0.851 0.080 9 108884801 intron variant T/C snv 0.92 4
rs662959
IL12A-AS1
0.851 0.080 3 159983443 intron variant G/A snv 0.16 4
rs677844
TNFRSF1B
0.851 0.080 1 12184261 intron variant T/C snv 0.22 4
rs7170924
IL16
0.851 0.080 15 81290798 intron variant G/T snv 0.30 4
rs8111742
MIRLET7E ; MIR99B ; SPACA6 ; SPACA6P-AS ; MIR125A
0.851 0.120 19 51692221 intron variant G/A;C snv 0.30 4
rs928508
NFYC ; MIR30C1
0.851 0.080 1 40757742 intron variant G/A;T snv 0.50 4
rs9535826
ATP7B
0.851 0.080 13 51991990 intron variant T/C;G snv 4
rs12051272
CDH13
0.925 0.120 16 82629683 intron variant G/C;T snv 3
rs13312840
NBN
0.882 0.120 8 89985681 intron variant A/G;T snv 3
rs1340420
TNKS2
0.925 0.080 10 91857549 intron variant A/G snv 0.71 0.70 3
rs1770474
TNKS2
0.925 0.080 10 91833770 intron variant G/A;T snv 3
rs181696
PLCH1
0.925 0.080 3 155548315 intron variant T/C snv 0.55 3
rs227060
C11orf65 ; ATM
0.882 0.160 11 108334154 intron variant C/T snv 0.27 3
rs2847153
TYMS
0.925 0.080 18 661647 intron variant G/A snv 0.22 3
rs3790622
IL19 ; IL10
0.882 0.320 1 206771818 intron variant G/A snv 1.5E-03 3
rs471692
TOP2A
0.925 0.080 17 40400518 intron variant T/A;C snv 0.79 3
rs4845882
C1orf167
0.882 0.120 1 11783110 intron variant A/G;T snv 3
rs7211777
STAT3
0.882 0.120 17 42382057 intron variant G/A snv 0.52 3
rs7741164
FOXP4-AS1
0.882 0.080 6 41525674 intron variant G/A snv 6.6E-02 3
rs9657904
CBLB ; LOC107986109
0.925 0.160 3 105867870 intron variant T/A;C snv 3
rs10845498
LRP6
0.925 0.080 12 12241640 intron variant G/A;C snv 2
rs11466345
TGFB1
1.000 0.080 19 41337556 intron variant T/C snv 0.12 2
rs11632964
SMAD3
1.000 0.080 15 67071235 intron variant C/G;T snv 2
rs1200399
BAZ1A
0.925 0.080 14 34823979 intron variant C/T snv 0.87 2
rs12541709
TNKS
1.000 0.080 8 9751081 intron variant C/G snv 0.29 2