Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs689465
PTGS2 ; PACERR
0.851 0.200 1 186681714 upstream gene variant T/C snv 0.14 7
rs2564978
CD55
0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs1801173
TP73
0.851 0.120 1 3682346 5 prime UTR variant C/T snv 0.20 0.18 5
rs2273953
TP73
0.851 0.120 1 3682336 5 prime UTR variant G/A;T snv 0.20; 3.3E-04 5
rs228729
PER3
0.827 0.120 1 7785635 intron variant T/C snv 0.69 0.69 5
rs760943842
ZNF436
0.851 0.080 1 23362976 missense variant G/A snv 4.0E-05 1.4E-05 5
rs1537514
C1orf167 ; MTHFR
0.882 0.120 1 11788011 missense variant G/C snv 0.10 0.10 4
rs60369023
CDA
0.851 0.240 1 20604981 missense variant G/A snv 2.6E-04 1.5E-04 4
rs677844
TNFRSF1B
0.851 0.080 1 12184261 intron variant T/C snv 0.22 4
rs928508
NFYC ; MIR30C1
0.851 0.080 1 40757742 intron variant G/A;T snv 0.50 4
rs267598140
DDR2
0.925 0.080 1 162778600 missense variant T/A;G snv 3
rs3790622
IL19 ; IL10
0.882 0.320 1 206771818 intron variant G/A snv 1.5E-03 3
rs4845882
C1orf167
0.882 0.120 1 11783110 intron variant A/G;T snv 3
rs772092699
EPHB2
0.925 0.080 1 22912497 missense variant C/A;G;T snv 4.0E-06 3
rs1048977
CDA
1.000 0.080 1 20618562 synonymous variant C/T snv 0.31 0.34 2
rs1049434
SLC16A1
0.925 0.120 1 112913924 missense variant A/T snv 0.59 0.66 2
rs1225118391
AGT
0.925 0.200 1 230710637 missense variant T/C snv 4.0E-06 2
rs228644
PER3
1.000 0.080 1 7806023 intron variant G/A snv 0.36 2
rs344924 1.000 0.080 1 67639770 intergenic variant A/G snv 0.17 2
rs560299246
EXO1
0.925 0.200 1 241858594 missense variant C/T snv 8.0E-05 7.0E-06 2
rs586339
KDM4A
1.000 0.080 1 43671586 missense variant C/A;G;T snv 0.70 0.78 2
rs707467
PER3
0.925 0.120 1 7801624 intron variant A/C snv 0.22 2
rs746983719
EXO1
0.925 0.200 1 241860647 missense variant T/C snv 1.2E-05 2
rs764493111
EXO1
0.925 0.200 1 241858654 missense variant G/A;T snv 8.0E-06; 8.0E-06 2
rs1077424
DAB1
1.000 0.080 1 57344632 intron variant G/C snv 0.52 1