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: rs11168249
rs11168249
HDAC7
9 0.807 0.120 12 47814585 intron variant T/C snv 0.50 0.700 1.000 2 2013 2016
dbSNP: rs1001007
rs1001007
CCR5AS
5 0.827 0.120 3 46387167 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1004234
rs1004234
IRF1-AS1 ; LINC02863
5 0.827 0.120 5 132421409 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10510607
rs10510607
CMC1
5 0.827 0.120 3 28244770 intron variant C/T snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs10743181
rs10743181 		5 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 0.700 1.000 1 2016 2016
dbSNP: rs10750899
rs10750899 		5 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 0.700 1.000 1 2016 2016
dbSNP: rs10761648
rs10761648
ZNF365
5 0.827 0.120 10 62594503 intron variant C/T snv 0.20 0.700 1.000 1 2016 2016
dbSNP: rs10775412
rs10775412
KSR1
5 0.827 0.120 17 27542007 intron variant A/C snv 0.30 0.700 1.000 1 2016 2016
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: rs11098964
rs11098964
ANTXR2
5 0.827 0.120 4 79966815 intron variant A/G;T snv 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: 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: 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: 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