Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13412852
LPIN1
0.851 0.120 2 11774815 intron variant C/T snv 0.26 4
rs3741981
OAS1
0.882 0.120 12 112911065 missense variant G/A;C snv 3
rs4619915
CXCL11 ; ART3
0.882 0.120 4 76034048 3 prime UTR variant A/G snv 0.61 3
rs17886084
MMP1 ; WTAPP1
1.000 0.080 11 102799765 intron variant C/- delins 2
rs267607117
TMEM67
0.925 0.080 8 93780747 missense variant G/T snv 2
rs1060500764
SMAD3
1.000 0.080 15 67181363 missense variant A/G snv 1
rs900837802
EIF2AK3
1.000 0.080 2 88595498 missense variant T/C snv 7.0E-06 1
rs9402373 1.000 0.080 6 131956291 intron variant C/A;G;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1430059719
MMP9
1.000 0.080 20 46012456 missense variant G/C snv 4.0E-06 1
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs781521972
SMAD2
1.000 0.080 18 47896706 synonymous variant T/A snv 4.0E-06 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1063303
TRIM5 ; TRIM22
0.925 0.120 11 5698520 missense variant G/A;C;T snv 4.0E-06; 0.50; 1.6E-05 2
rs1208663703
TMPRSS6
0.763 0.200 22 37086414 missense variant T/C snv 5.2E-06 7.0E-06 9
rs1161457931
TMPRSS6
0.763 0.200 22 37084836 missense variant C/T snv 6.4E-06 9
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs267606959
POLG
0.732 0.200 15 89318986 missense variant G/A snv 2.0E-05 19
rs5496
ICAM1
1.000 0.080 19 10284771 intron variant G/A snv 7.8E-03 3.3E-02 1
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs7080536
HABP2 ; NRAP
0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800471
TGFB1
0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26