Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs9402373 1.000 0.080 6 131956291 intron variant C/A;G;T snv 1
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs3921
CXCL10 ; ART3
0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs4619915
CXCL11 ; ART3
0.882 0.120 4 76034048 3 prime UTR variant A/G snv 0.61 3
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs900837802
EIF2AK3
1.000 0.080 2 88595498 missense variant T/C snv 7.0E-06 1
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs11558492
GNPAT
0.827 0.200 1 231272345 missense variant A/G;T snv 0.16 5
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs7080536
HABP2 ; NRAP
0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs5496
ICAM1
1.000 0.080 19 10284771 intron variant G/A snv 7.8E-03 3.3E-02 1
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs10833
IL15
0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10