Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs1800972
DEFB1
0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs10421768
HAMP
0.807 0.120 19 35281996 intron variant A/G snv 0.21 6
rs1800870
ALDH3A2
0.851 0.200 17 19649164 intron variant C/T snv 5
rs1978331
LTA4H
0.827 0.200 12 96015423 intron variant A/G snv 0.50 5
rs373950030
CD209
0.882 0.080 19 7744967 missense variant C/T snv 2.0E-05 2.1E-05 3
rs2243268
IL4
0.882 0.040 5 132678271 intron variant A/C snv 0.23 3
rs2243274
IL4 ; LOC105379176
0.882 0.080 5 132679140 intron variant G/A snv 0.34 3
rs2367707
EREG
0.925 0.080 4 74382717 synonymous variant A/G snv 0.79 0.79 2
rs2540474 1.000 0.040 12 96054069 intergenic variant A/G snv 0.48 1
rs6446993
EREG
1.000 0.040 4 74366149 intron variant A/G;T snv 1