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: rs10800314
rs10800314 		5 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 0.700 1.000 1 2016 2016
dbSNP: rs10870077
rs10870077
CARD9
5 0.827 0.120 9 136369439 intron variant C/G snv 0.38 0.700 1.000 1 2016 2016
dbSNP: rs10889676
rs10889676
IL23R
5 0.827 0.120 1 67256884 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10995271
rs10995271 		8 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 0.700 1.000 1 2016 2016
dbSNP: rs11098964
rs11098964
ANTXR2
5 0.827 0.120 4 79966815 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11117431
rs11117431 		6 0.807 0.160 16 85981710 intron variant A/G snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs111305875
rs111305875 		5 0.827 0.120 6 167098098 intron variant T/G snv 3.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs11190133
rs11190133 		5 0.827 0.120 10 99518968 intergenic variant C/T snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs11221322
rs11221322
ETS1
5 0.827 0.120 11 128476898 intron variant T/C snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs11221332
rs11221332
ETS1
13 0.763 0.280 11 128511079 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11229555
rs11229555
GLYAT
7 0.827 0.120 11 58641214 intron variant G/T snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs11230563
rs11230563
CD6 ; LOC105369326
8 0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 0.700 1.000 1 2016 2016
dbSNP: rs11236797
rs11236797 		8 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 0.700 1.000 1 2016 2016
dbSNP: rs11306716
rs11306716 		5 0.827 0.120 2 203843041 intergenic variant T/-;TT delins 0.700 1.000 1 2016 2016
dbSNP: rs114202211
rs114202211
HIPK1
5 0.827 0.120 1 113943285 intron variant T/C snv 8.1E-03 0.700 1.000 1 2016 2016
dbSNP: rs11574938
rs11574938
ITGAL
6 0.827 0.120 16 30474072 missense variant G/A;C snv 0.62 0.700 1.000 1 2016 2016
dbSNP: rs116046827
rs116046827
BSN
5 0.827 0.120 3 49618715 intron variant T/C snv 8.6E-03 0.700 1.000 1 2016 2016
dbSNP: rs11614178
rs11614178
IFNG-AS1 ; LOC107984526
6 0.827 0.120 12 68114342 intron variant G/A;T snv 0.26 0.700 1.000 1 2016 2016
dbSNP: rs11616188
rs11616188 		5 0.827 0.120 12 6393576 upstream gene variant G/A snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs11624293
rs11624293
LINC01147
5 0.827 0.120 14 88022477 intron variant T/C snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs11632488
rs11632488 		1 1.000 0.040 15 79975159 upstream gene variant A/G snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs11649613
rs11649613
LOC107984859
5 0.827 0.120 16 11225500 downstream gene variant C/T snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs11675538
rs11675538 		5 0.827 0.120 2 65459327 intron variant C/T snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs11676348
rs11676348 		8 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11691685
rs11691685
TEX41
5 0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02 0.700 1.000 1 2016 2016