Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 5
rs10553577
STAT4
1.000 0.200 2 191090464 intron variant ATAATA/-;ATA;ATAATAATA delins 1
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs1085308048
PTEN
0.851 0.320 10 87933175 stop gained T/G snv 6
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11048434
KLRG1
1.000 0.200 12 9001336 intron variant G/A snv 0.28 1
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs115575857 1.000 0.200 6 32691868 regulatory region variant A/G snv 1
rs116855232
NUDT15
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs11805303
C1orf141 ; IL23R
0.827 0.240 1 67209833 intron variant C/T snv 0.30 6
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs1507153 1.000 0.200 6 78774669 intergenic variant C/A snv 0.32 1
rs17074492
LOC105370283
1.000 0.200 13 81587764 intergenic variant C/A;T snv 1
rs17339836
TNPO3
1.000 0.200 7 129041008 intron variant C/T snv 9.0E-02 1
rs1957173 1.000 0.200 14 45937713 intron variant C/T snv 4.6E-02 1
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs2736345
BLK
0.882 0.280 8 11494976 intron variant A/G snv 0.35 3
rs3135394
HLA-DRA
0.851 0.240 6 32440720 intron variant A/G snv 6.3E-02 4