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: rs3024505
rs3024505 		10 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.800 1.000 3 2009 2015
dbSNP: rs1015166
rs1015166
TAP2
2 0.925 0.120 6 32830954 intron variant C/G;T snv 0.28 0.800 1.000 2 2007 2015
dbSNP: rs1270942
rs1270942
CFB ; CYP21A2
11 0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 0.800 1.000 2 2007 2015
dbSNP: rs12927355
rs12927355
CLEC16A
3 0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 0.800 1.000 2 2011 2015
dbSNP: rs1980493
rs1980493
BTNL2 ; TSBP1-AS1
10 0.776 0.400 6 32395438 intron variant T/C snv 0.13 0.800 1.000 2 2007 2015
dbSNP: rs2251396
rs2251396
MICA-AS1
5 0.827 0.240 6 31396930 upstream gene variant G/A snv 0.24 0.800 1.000 2 2007 2015
dbSNP: rs2304256
rs2304256
TYK2
13 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 0.800 1.000 2 2010 2011
dbSNP: rs2523989
rs2523989
TRIM31 ; TRIM31-AS1
5 0.827 0.280 6 30110498 missense variant C/T snv 0.12 0.12 0.800 1.000 2 2007 2015
dbSNP: rs2857595
rs2857595 		9 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 0.800 1.000 2 2007 2015
dbSNP: rs3825932
rs3825932
CTSH
6 0.827 0.360 15 78943104 intron variant T/C snv 0.50 0.800 1.000 2 2008 2009
dbSNP: rs4788084
rs4788084
IL27
6 0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 0.800 1.000 2 2009 2011
dbSNP: rs61839660
rs61839660
IL2RA
9 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 0.800 1.000 2 2012 2015
dbSNP: rs7111341
rs7111341 		2 0.925 0.120 11 2191936 regulatory region variant C/T snv 0.29 0.800 1.000 2 2007 2009
dbSNP: rs8056814
rs8056814
CTRB1
2 0.925 0.160 16 75218429 upstream gene variant G/A snv 0.16 0.800 1.000 2 2011 2015
dbSNP: rs886424
rs886424
LINC00243
10 0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 0.800 1.000 2 2007 2015
dbSNP: rs10517086
rs10517086
LINC02357
4 0.882 0.160 4 26083889 intron variant G/A snv 0.27 0.800 1.000 1 2009 2009
dbSNP: rs10786436
rs10786436
HPSE2
1 1.000 0.120 10 98540425 intron variant C/T snv 0.40 0.800 1.000 1 2011 2011
dbSNP: rs11052552
rs11052552
LINC02390
1 1.000 0.120 12 9703362 upstream gene variant T/G snv 0.42 0.800 1.000 1 2007 2007
dbSNP: rs11258747
rs11258747
PRKCQ
1 1.000 0.120 10 6430929 missense variant G/C;T snv 4.0E-06; 0.17 0.800 1.000 1 2009 2009
dbSNP: rs12251307
rs12251307 		1 1.000 0.120 10 6081532 intergenic variant C/T snv 0.18 0.800 1.000 1 2009 2009
dbSNP: rs12444268
rs12444268 		1 1.000 0.120 16 20331250 upstream gene variant T/A snv 0.22 0.800 1.000 1 2009 2009
dbSNP: rs12679857
rs12679857
COLEC10
1 1.000 0.120 8 118965098 intergenic variant A/G snv 0.36 0.800 1.000 1 2011 2011
dbSNP: rs1465788
rs1465788
ZFP36L1
2 0.925 0.160 14 68796882 upstream gene variant T/C snv 0.70 0.800 1.000 1 2009 2009
dbSNP: rs16956936
rs16956936
DNAH2
1 1.000 0.120 17 7730374 intron variant C/A;T snv 0.800 1.000 1 2009 2009
dbSNP: rs2269241
rs2269241
PGM1
2 1.000 0.120 1 63643100 intron variant T/C snv 0.23 0.800 1.000 1 2009 2009