Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35597970
MFSD13A ; ACTR1A
1.000 0.120 10 102469300 intron variant -/A delins 0.46 1
rs35350651
ATXN2
1.000 0.120 12 111469627 3 prime UTR variant -/C ins 0.66 1
rs7753873
LOC107986649 ; WAKMAR2
0.882 0.320 6 137852285 intron variant A/C snv 0.18 3
rs12597084
RBFOX1
1.000 0.120 16 5769619 intron variant A/C snv 0.67 1
rs1310182
AP4B1-AS1 ; PTPN22
0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs17855750
IL27
0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs77041280
HRH4
0.925 0.160 18 24477516 missense variant A/C;T snv 2
rs2149039
BSND
1.000 0.120 1 55014701 3 prime UTR variant A/C;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs3819024
IL17A
0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs721917
SFTPD
0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs569108
MS4A2
0.790 0.200 11 60095631 missense variant A/G snv 4.7E-02 7.3E-02 8
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 5
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19 4
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 4
rs1887415
IFNGR1
0.882 0.160 6 137198101 missense variant A/G snv 5.1E-02 1.8E-02 3