Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs6964969
IKZF1
0.851 0.120 7 50405553 downstream gene variant A/G snv 0.23 4
rs11770117 1.000 0.120 7 50406065 downstream gene variant A/T snv 0.41 2
rs12719019 1.000 0.120 7 50408441 downstream gene variant C/T snv 0.40 2
rs6944602 0.925 0.120 7 50406053 downstream gene variant G/A;T snv 2
rs8015478
CEBPE
1.000 0.120 14 23116809 downstream gene variant A/C snv 0.68 2
rs12887958 1.000 0.120 14 23113360 downstream gene variant C/T snv 0.37 1
rs4982731 1.000 0.120 14 23116124 downstream gene variant C/T snv 0.68 1
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs2239633
CEBPE
0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 12
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs17079534 1.000 0.120 3 39805581 upstream gene variant G/A;C snv 1
rs1945213 1.000 0.120 11 56408195 upstream gene variant C/G;T snv 1
rs4982729 1.000 0.120 14 23107402 upstream gene variant T/C snv 0.66 1
rs637868
PHGDH
1.000 0.120 1 119714487 splice region variant T/C snv 0.56 3
rs4132601
IKZF1
0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 9
rs149940960
GREB1
1.000 0.120 2 11641492 3 prime UTR variant T/C snv 1.0E-02 3
rs41307935
ZDHHC18
1.000 0.120 1 26854576 3 prime UTR variant C/T snv 6.1E-02 3
rs10949482
NHLRC1
1.000 0.120 6 18121083 3 prime UTR variant C/T snv 6.8E-02 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs738408
PNPLA3
0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22 10
rs12669559
IKZF1
1.000 0.120 7 50368079 synonymous variant T/G snv 0.35 0.32 3
rs408626
DHFR ; MSH3
0.925 0.120 5 80655314 non coding transcript exon variant T/C snv 0.48 2
rs4947709
GRB10
1.000 0.120 7 50605210 non coding transcript exon variant T/C snv 0.63 1