Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3805500
DROSHA
1.000 0.120 5 31462870 intron variant G/A snv 0.60 1
rs9308731
BCL2L11 ; MIR4435-2HG
0.925 0.120 2 111150685 intron variant G/A snv 0.59 2
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs228014
ASTN1
1.000 0.120 1 177002472 intron variant T/C snv 0.58 1
rs6586163
FAS ; FAS-AS1 ; ACTA2
0.925 0.120 10 88992261 non coding transcript exon variant A/C snv 0.58 2
rs7690934
LEF1
0.925 0.120 4 108104709 intron variant T/C snv 0.57 2
rs1292034
RPS6KB1
0.882 0.160 17 59912499 intron variant G/A snv 0.56 3
rs888096
LOC107985868
0.925 0.120 2 37376658 downstream gene variant G/A snv 0.55 2
rs8113877 1.000 0.120 20 46006406 upstream gene variant G/T snv 0.55 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs4869818
OPRM1
0.925 0.120 6 154150090 intron variant G/A snv 0.54 2
rs2236256
IPCEF1 ; OPRM1
0.925 0.120 6 154157305 3 prime UTR variant C/A snv 0.52 2
rs391855 0.925 0.120 16 85895015 upstream gene variant A/T snv 0.52 2
rs9270750
HLA-DRB1
0.925 0.120 6 32600569 intergenic variant G/A snv 0.52 2
rs8024033 0.925 0.120 15 40111456 upstream gene variant C/G snv 0.50 2
rs2147420
FAS
1.000 0.120 10 88999856 intron variant A/G snv 0.50 1
rs4406737
FAS
0.925 0.120 10 88999967 intron variant A/G snv 0.50 2
rs391023 0.925 0.120 16 85894208 upstream gene variant C/T snv 0.48 2
rs7944004 0.925 0.120 11 2289922 intergenic variant T/G snv 0.48 2
rs2267708
GPR37
0.925 0.120 7 124752458 intron variant C/T snv 0.47 2
rs806321
DLEU1
0.851 0.160 13 50267187 intron variant C/T snv 0.47 4
rs3769825
CASP8
0.925 0.120 2 201246657 intron variant A/G snv 0.46 2
rs10028805
BANK1
0.882 0.160 4 101816093 intron variant G/A snv 0.45 3
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106