Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 10
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs2006996 0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02 4
rs11554257 1.000 0.040 9 114842790 upstream gene variant T/C snv 0.13 2
rs13300483
DELEC1
1.000 0.080 9 114881082 intron variant C/T snv 0.21 2
rs11641184
LITAF
0.925 0.040 16 11610795 intron variant C/A snv 0.36 3
rs38904 1.000 0.120 7 117252792 intergenic variant T/C snv 0.52 2
rs6828740
RPSAP35
1.000 0.120 4 117413463 non coding transcript exon variant T/C snv 5.8E-02 2
rs200829864
TLR4
9 117704494 missense variant G/A;T snv 2.1E-05 1
rs5030728
TLR4
0.807 0.160 9 117712004 intron variant G/A;T snv 0.23 7
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs630923
CXCR5
1.000 0.080 11 118883644 upstream gene variant C/A snv 0.13 2
rs11064881
CIT
1.000 0.040 12 119709120 intron variant G/A snv 5.0E-02 3
rs3814055
NR1I2
0.925 0.040 3 119781188 5 prime UTR variant C/T snv 0.35 4
rs6785049
NR1I2
0.882 0.080 3 119814886 intron variant G/A;T snv 0.46 4
rs2276707
NR1I2
0.925 0.040 3 119815306 intron variant C/G;T snv 4.1E-04; 0.24 3
rs7657746
KIAA1109
0.925 0.040 4 122240464 intron variant A/G snv 0.24 3
rs1479918
ADAD1
1.000 0.040 4 122430276 downstream gene variant A/T snv 0.19 2
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131