Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069727
IFNG ; IFNG-AS1
0.763 0.320 12 68154443 intron variant T/A;C snv 9
rs4132601
IKZF1
0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 9
rs1966862
ARHGAP24
0.790 0.120 4 85766908 intron variant A/G snv 0.14 8
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs3135388
HLA-DRA
0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 7
rs924607
LOC105374608 ; LOC100996325
0.851 0.120 5 609978 intron variant C/T snv 0.32 7
rs1057519743
CRLF2
0.827 0.120 Y 1196852 missense variant A/C snv 6
rs2413739
PACSIN2
0.827 0.120 22 43001030 intron variant C/T snv 0.43 6
rs724159947
ETV6
0.851 0.120 12 11869601 missense variant C/T snv 6
rs797045145
HFE ; LOC108783645
0.807 0.240 6 26091479 stop gained G/A snv 6
rs9479
PML
0.851 0.120 15 74036235 3 prime UTR variant A/G snv 0.50 6
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
rs587781823
ATM
0.851 0.280 11 108284370 frameshift variant -/T delins 5
rs6021191
NFATC2
0.851 0.120 20 51419700 intron variant A/T snv 4.9E-02 5
rs979090956
ABCB1
0.827 0.200 7 87553822 missense variant G/C snv 5
rs10106
FPGS
0.851 0.200 9 127813796 3 prime UTR variant T/C snv 0.45 4
rs1544105
FPGS
0.851 0.200 9 127800446 intron variant C/T snv 0.48 4
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 4
rs17069665
FOXO3
0.882 0.120 6 108620265 intron variant A/C;G snv 4
rs4646450
CYP3A5 ; ZSCAN25
0.882 0.120 7 99668695 3 prime UTR variant G/A snv 0.38 4
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 4
rs569954362
SLC19A1
0.851 0.160 21 45530871 synonymous variant G/A snv 4
rs6535455
HPSE
0.851 0.160 4 83310951 intron variant T/A;C snv 4
rs6964969
IKZF1
0.851 0.120 7 50405553 downstream gene variant A/G snv 0.23 4
rs7088318
PIP4K2A
0.851 0.120 10 22564019 intron variant C/A snv 0.55 4