Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17886084
MMP1 ; WTAPP1
1.000 0.080 11 102799765 intron variant C/- delins 2
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800471
TGFB1
0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs236918
PCSK7
0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs267606959
POLG
0.732 0.200 15 89318986 missense variant G/A snv 2.0E-05 19
rs267607117
TMEM67
0.925 0.080 8 93780747 missense variant G/T snv 2
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs3194051
IL7R
0.851 0.200 5 35876172 missense variant A/G snv 0.24 0.28 4
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs3741981
OAS1
0.882 0.120 12 112911065 missense variant G/A;C snv 3
rs3921
CXCL10 ; ART3
0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs4619915
CXCL11 ; ART3
0.882 0.120 4 76034048 3 prime UTR variant A/G snv 0.61 3
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223