Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4581
APOH
0.851 0.160 17 66214639 missense variant C/A;G snv 0.38; 4.0E-06; 4.0E-06 0.36 5
rs28362930
SEMA7A
0.925 0.160 15 74408859 downstream gene variant G/A snv 0.16 3
rs3181032
IFNG-AS1
0.925 0.160 12 68162395 intron variant A/C snv 5.3E-02 2
rs3805455
GABRP
0.925 0.160 5 170813490 3 prime UTR variant T/C snv 0.50 2
rs929763
LOC107986475 ; GABRP
0.925 0.160 5 170783993 intron variant A/T snv 0.72 2
rs10489265
TNFSF4 ; LOC100506023
0.827 0.200 1 173266926 regulatory region variant A/C snv 0.21 5
rs1051169
S100B
0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65 5
rs2243188
LOC105372878 ; IL19
0.851 0.200 1 206841127 intron variant A/C;T snv 0.69 4
rs280500
TYK2
0.882 0.200 19 10379726 5 prime UTR variant A/G snv 0.20 3
rs741761
SEMA7A ; MIR6881
0.882 0.200 15 74411588 missense variant T/A;C snv 1.8E-04; 0.35 3
rs12720270
TYK2
0.851 0.240 19 10365084 intron variant G/A snv 0.21 0.16 4
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 7
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs2069705
IFNG-AS1 ; IFNG
0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs3077
HLA-DPA1
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs9277535
HLA-DPB1
0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs549908
IL18
0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14