Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1085308048
rs1085308048
PTEN
6 0.851 0.320 10 87933175 stop gained T/G snv 0.010 1.000 1 1998 1998
dbSNP: rs1004819
rs1004819
IL23R ; C1orf141
9 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.010 1.000 1 2009 2009
dbSNP: rs10489629
rs10489629
IL23R ; C1orf141
5 0.827 0.240 1 67222666 intron variant T/C snv 0.48 0.010 1.000 1 2009 2009
dbSNP: rs10889677
rs10889677
IL23R
40 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.010 1.000 1 2009 2009
dbSNP: rs11209026
rs11209026
IL23R
46 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2009 2009
dbSNP: rs11209032
rs11209032 		10 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 0.010 1.000 1 2009 2009
dbSNP: rs11805303
rs11805303
IL23R ; C1orf141
6 0.827 0.240 1 67209833 intron variant C/T snv 0.30 0.010 1.000 1 2009 2009
dbSNP: rs2201841
rs2201841
IL23R ; C1orf141
14 0.716 0.440 1 67228519 intron variant A/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs7517847
rs7517847
IL23R ; C1orf141
19 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.010 1.000 1 2009 2009
dbSNP: rs7530511
rs7530511
IL23R ; C1orf141
12 0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 0.010 1.000 1 2009 2009
dbSNP: rs1143634
rs1143634
IL1B
52 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 0.010 1.000 1 2011 2011
dbSNP: rs8192284
rs8192284
IL6R
19 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2011 2011
dbSNP: rs774359492
rs774359492
WDHD1
7 0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs10168266
rs10168266
STAT4
8 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.800 1.000 1 2013 2013
dbSNP: rs10553577
rs10553577
STAT4
1 1.000 0.200 2 191090464 intron variant ATAATA/-;ATA;ATAATAATA delins 0.700 1.000 1 2013 2013
dbSNP: rs115575857
rs115575857 		1 1.000 0.200 6 32691868 regulatory region variant A/G snv 0.700 1.000 1 2013 2013
dbSNP: rs1507153
rs1507153 		1 1.000 0.200 6 78774669 intergenic variant C/A snv 0.32 0.700 1.000 1 2013 2013
dbSNP: rs17339836
rs17339836
TNPO3
1 1.000 0.200 7 129041008 intron variant C/T snv 9.0E-02 0.700 1.000 1 2013 2013
dbSNP: rs2431098
rs2431098 		5 0.827 0.240 5 160460329 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2736345
rs2736345
BLK
3 0.882 0.280 8 11494976 intron variant A/G snv 0.35 0.700 1.000 1 2013 2013
dbSNP: rs3135394
rs3135394
HLA-DRA
4 0.851 0.240 6 32440720 intron variant A/G snv 6.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs359457
rs359457 		2 0.925 0.240 5 173852839 intergenic variant C/T snv 0.59 0.700 1.000 1 2013 2013
dbSNP: rs3757387
rs3757387
IRF5
6 0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs4282438
rs4282438
COL11A2P1
6 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 0.800 1.000 1 2013 2013
dbSNP: rs485497
rs485497
IL12A-AS1
2 0.925 0.200 3 160001345 intron variant A/C;G snv 0.700 1.000 1 2013 2013