Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1800566
NQO1
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs121912594
CPS1
0.882 0.160 2 210675762 missense variant A/C snv 7
rs11465996
LY96
0.790 0.240 8 73989727 upstream gene variant C/G snv 0.25 7
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02 6
rs1384936174
NOD2
0.827 0.040 16 50710812 missense variant G/A;T snv 4.0E-06; 4.0E-06 6
rs2071747
HMOX1
0.851 0.120 22 35381192 missense variant G/C snv 4.3E-02 4.1E-02 4
rs10505232 0.925 0.040 8 114878275 intergenic variant A/C snv 0.11 3
rs3181382
ADCY4
0.925 0.040 14 24320104 intron variant G/C;T snv 3
rs2241712
B9D2 ; TMEM91
0.882 0.120 19 41363851 intron variant C/T snv 0.71 3
rs9927732
BANP
0.925 0.040 16 88043118 intron variant C/A;G;T snv 3
rs1384663432
CARD8
0.925 0.040 19 48218886 missense variant T/C snv 2
rs1048719
GM2A
0.925 0.080 5 151253271 missense variant G/A snv 6.1E-02 3.7E-02 2
rs2075783
GM2A
0.925 0.080 5 151267219 3 prime UTR variant A/C snv 0.22 2
rs4912711
HBEGF
1.000 0.040 5 140338940 intron variant G/T snv 0.12 1
rs117739035
SIGIRR
1.000 0.040 11 408174 missense variant G/T snv 2.9E-02 2.5E-02 1