Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3761549
FOXP3
0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 18
rs1131445
IL16 ; STARD5
0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv 16
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs2072472
IL1R2
0.732 0.200 2 102026557 intron variant A/G snv 0.24 13
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs1550117
DNMT3A
0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs4957014
AHRR ; PDCD6
0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs1181860747
INSR
0.776 0.240 19 7122961 missense variant C/T snv 10
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs3756712
PDCD6 ; AHRR
0.790 0.160 5 308981 non coding transcript exon variant A/C;T snv 10
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 10
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs1834306
MIR10526 ; MIR100 ; MIR100HG
0.776 0.200 11 122152479 intron variant A/G snv 0.49 9
rs2280883
FOXP3
0.827 0.280 X 49252667 intron variant T/C snv 0.30 9
rs2856836
IL1A
0.763 0.280 2 112774506 3 prime UTR variant A/G snv 0.26 9
rs710886
LOC105375751 ; PCAT1
0.763 0.160 8 127014615 intron variant C/T snv 0.37 9
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77 9
rs1037189404
MUC1
0.776 0.280 1 155187519 missense variant C/T snv 8
rs11031006
LOC105376607
0.882 0.120 11 30204981 intron variant G/A snv 0.11 8
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 8
rs766333007
MUC1
0.776 0.280 1 155192274 missense variant C/T snv 7.0E-06 8
rs7907606 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 8
rs9582036
FLT1
0.776 0.280 13 28311271 intron variant C/A snv 0.59 8
rs1536309
MIR146B
0.851 0.160 10 102435445 upstream gene variant A/G snv 0.32 7
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 6