Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10044354
LNPEP
1.000 0.040 5 96984791 intron variant C/T snv 0.41 1
rs1048709
CFB ; CYP21A2
0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs2075800
HSPA1L
0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 8
rs1040461
RAB23
1.000 0.040 6 57190556 missense variant C/T snv 9.8E-02 0.12 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs377679652
GRB10
0.925 0.040 7 50669861 missense variant C/T snv 4.6E-05 2.8E-05 2
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs12722489
IL2RA
0.882 0.160 10 6060049 intron variant C/T snv 0.11 3
rs61860052
ANXA11
0.925 0.080 10 80201955 intron variant C/A snv 6.4E-02 2
rs1128334
ETS1
0.851 0.160 11 128459064 3 prime UTR variant C/T snv 0.11 5
rs10893872 0.882 0.120 11 128455658 downstream gene variant T/C snv 0.44 4
rs397514601
CAPN5
0.882 0.040 11 77115423 missense variant G/A;T snv 4.0E-06 3
rs703842
METTL1 ; CYP27B1
0.851 0.240 12 57768956 missense variant A/G snv 0.38 0.33 4
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 6
rs104895462
NOD2
0.882 0.120 16 50710911 missense variant C/T snv 3
rs104895460
NOD2
0.925 0.080 16 50711316 missense variant C/T snv 2
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38