Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs704840
LOC100506023 ; TNFSF4
0.851 0.240 1 173257056 intergenic variant T/G snv 0.29 4
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs9523762
LOC105370315 ; GPC5
0.925 0.120 13 92679633 intron variant G/A snv 0.39 2
rs2887502
LOC105375914
0.925 0.120 8 78844356 intron variant C/T snv 0.69 2
rs12044852
LOC105378925 ; CD58
0.925 0.120 1 116545157 intron variant C/A snv 0.12 2
rs703842
METTL1 ; CYP27B1
0.851 0.240 12 57768956 missense variant A/G snv 0.38 0.33 4
rs2300747
MIR548AC ; CD58
0.882 0.200 1 116561593 intron variant A/G snv 0.19 3
rs422951
NOTCH4
0.807 0.280 6 32220606 missense variant T/C snv 0.40 0.40 8
rs1520333
PKIA-AS1 ; LOC105375911
0.925 0.120 8 78488803 intron variant A/G snv 0.40 2
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs7601754
STAT4
0.882 0.160 2 191075725 intron variant G/A;T snv 3
rs13426947
STAT4
0.925 0.200 2 191068528 3 prime UTR variant G/A snv 0.20 2
rs767455
TNFRSF1A
0.742 0.400 12 6341779 synonymous variant T/C snv 0.37 0.40 13
rs1800693
TNFRSF1A
0.776 0.360 12 6330843 non coding transcript exon variant T/C snv 0.36; 4.0E-06 0.38 9
rs4149577
TNFRSF1A
0.827 0.280 12 6338356 intron variant G/A;T snv 7
rs1234315
TNFSF4
0.807 0.400 1 173209324 upstream gene variant C/T snv 0.57 6
rs844648
TNFSF4 ; LOC100506023
0.807 0.280 1 173254724 regulatory region variant G/A snv 0.46 6
rs1150757
TNXB
0.925 0.160 6 32061428 synonymous variant G/A;C snv 5.9E-02 2