Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7572733
PLCL1
0.925 0.120 2 198065082 intron variant C/T snv 0.43 4
rs1518364
PLCL1
0.925 0.120 2 197945251 intron variant G/A snv 0.49 3
rs17000730
TYK2
0.882 0.120 19 10380572 5 prime UTR variant T/C snv 5.0E-03 3
rs280501
TYK2
0.882 0.120 19 10380646 upstream gene variant C/T snv 0.20 3
rs938929
PLCL1
0.925 0.120 2 197916136 intron variant A/G snv 0.50 3
rs9986765
PIP
0.925 0.120 7 143138146 intron variant A/G snv 0.12 3
rs3750716
CPN1
0.925 0.120 10 100057106 synonymous variant C/G;T snv 6.6E-03 2
rs7750458
HLA-DPA1 ; HLA-DPB1
0.925 0.120 6 33077921 intron variant G/A snv 9.5E-02 2
rs9500928
HLA-DPB1 ; HLA-DPA1
0.925 0.120 6 33081917 intron variant C/T snv 4.0E-02 2
rs2492358 0.851 0.160 9 34737831 intron variant C/T snv 0.78 5
rs3129843 0.827 0.160 6 32427949 intergenic variant A/G snv 6.3E-02 5
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 7
rs6738825
PLCL1
0.851 0.200 2 198032171 intron variant A/G snv 0.49 5
rs9501251
HLA-DPA1 ; HLA-DPB1
0.882 0.200 6 33081886 intron variant A/G snv 4.0E-02 3
rs1800451
MBL2
0.776 0.240 10 52771466 missense variant C/T snv 3.2E-02 7.9E-02 9
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 8
rs3733197
BANK1
0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs11171739
ERBB3
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 10
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 10
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs5030737
MBL2
0.752 0.360 10 52771482 missense variant G/A snv 5.6E-02 5.0E-02 11
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19