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: rs879253743
rs879253743
NPAS2 ; NPAS2-AS1
1 1.000 0.040 2 100975538 missense variant C/A;G snv 0.700 0
dbSNP: rs7166401
rs7166401
CHSY1
1 1.000 0.040 15 101235913 intron variant A/G snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
99 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2019 2019
dbSNP: rs11937871
rs11937871 		1 1.000 0.040 4 103871299 upstream gene variant C/T snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs821693
rs821693 		1 1.000 0.040 10 106360432 intergenic variant A/G;T snv 0.87 0.700 1.000 1 2011 2011
dbSNP: rs12097821
rs12097821 		4 0.882 0.040 1 106793679 regulatory region variant G/A;T snv 0.720 0.500 2 2011 2015
dbSNP: rs7317862
rs7317862
FAM155A
1 1.000 0.040 13 107253690 intron variant A/C snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs876660612
rs876660612
APC
1 1.000 0.040 5 112819236 missense variant C/T snv 0.010 1.000 1 2017 2017
dbSNP: rs7099208
rs7099208
FAM160B1
1 1.000 0.040 10 114894815 intron variant A/G snv 0.36 0.010 1.000 1 2014 2014
dbSNP: rs78655421
rs78655421
CFTR
18 0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 0.010 1.000 1 2017 2017
dbSNP: rs3731611
rs3731611
MARCO
1 1.000 0.040 2 118985035 intron variant G/A;T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs4959523
rs4959523 		1 1.000 0.040 6 1193180 intergenic variant A/G snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs2501443
rs2501443 		1 1.000 0.040 7 122902383 intergenic variant A/G snv 0.47 0.700 1.000 1 2011 2011
dbSNP: rs7802723
rs7802723 		1 1.000 0.040 7 138244561 intergenic variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs6578134
rs6578134
PTK2
1 1.000 0.040 8 140768335 intron variant C/T snv 4.2E-02 0.700 1.000 1 2011 2011
dbSNP: rs967004
rs967004 		1 1.000 0.040 4 141923771 intergenic variant G/A snv 0.73 0.700 1.000 1 2011 2011
dbSNP: rs852977
rs852977
NR3C1
1 1.000 0.040 5 143307929 intron variant A/G snv 0.29 0.010 1.000 1 2016 2016
dbSNP: rs312620
rs312620 		1 1.000 0.040 5 143980913 intergenic variant T/A snv 4.2E-02 0.700 1.000 1 2011 2011
dbSNP: rs5951785
rs5951785
MIR506 ; LOC105373347
1 1.000 0.040 X 147230358 intron variant A/G snv 0.32 0.010 1.000 1 2016 2016
dbSNP: rs1447393
rs1447393
MIR510 ; LOC105373347
1 1.000 0.040 X 147272022 downstream gene variant C/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs253296
rs253296 		1 1.000 0.040 5 150573187 intergenic variant G/A snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs11204885
rs11204885
TDRKH
1 1.000 0.040 1 151775494 missense variant A/G;T snv 0.23 0.20 0.700 1.000 1 2011 2011
dbSNP: rs11918142
rs11918142
IL12A-AS1
1 1.000 0.040 3 160189298 intron variant T/C snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs7023221
rs7023221 		1 1.000 0.040 9 16085264 intergenic variant T/C snv 0.48 0.700 1.000 1 2011 2011
dbSNP: rs163065
rs163065
LINC02150
1 1.000 0.040 5 16434781 intron variant G/A;C;T snv 0.700 1.000 1 2011 2011