Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9402373 1.000 0.080 6 131956291 intron variant C/A;G;T snv 1
rs900837802
EIF2AK3
1.000 0.080 2 88595498 missense variant T/C snv 7.0E-06 1
rs5496
ICAM1
1.000 0.080 19 10284771 intron variant G/A snv 7.8E-03 3.3E-02 1
rs1430059719
MMP9
1.000 0.080 20 46012456 missense variant G/C snv 4.0E-06 1
rs781521972
SMAD2
1.000 0.080 18 47896706 synonymous variant T/A snv 4.0E-06 1
rs1060500764
SMAD3
1.000 0.080 15 67181363 missense variant A/G snv 1
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
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
rs4619915
CXCL11 ; ART3
0.882 0.120 4 76034048 3 prime UTR variant A/G snv 0.61 3
rs3741981
OAS1
0.882 0.120 12 112911065 missense variant G/A;C snv 3
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs3194051
IL7R
0.851 0.200 5 35876172 missense variant A/G snv 0.24 0.28 4
rs10336
LOC101928809 ; CXCL9
0.851 0.240 4 76001835 3 prime UTR variant A/G;T snv 4
rs13412852
LPIN1
0.851 0.120 2 11774815 intron variant C/T snv 0.26 4
rs11558492
GNPAT
0.827 0.200 1 231272345 missense variant A/G;T snv 0.16 5
rs14158
LDLR
0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 5
rs16851720
RNF7
0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs17047200
TLL1
0.827 0.200 4 166008836 intron variant A/T snv 0.18 5
rs3921
CXCL10 ; ART3
0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs1161457931
TMPRSS6
0.763 0.200 22 37084836 missense variant C/T snv 6.4E-06 9
rs1208663703
TMPRSS6
0.763 0.200 22 37086414 missense variant T/C snv 5.2E-06 7.0E-06 9
rs10833
IL15
0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10