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: rs254560
rs254560
C5orf66
2 1.000 0.040 5 135107916 intron variant G/A snv 0.32 0.800 1.000 4 2011 2017
dbSNP: rs11150589
rs11150589
ITGAL
2 1.000 0.040 16 30471173 upstream gene variant T/A;C;G snv 0.800 1.000 3 2012 2017
dbSNP: rs12568930
rs12568930 		4 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 0.800 1.000 3 2009 2017
dbSNP: rs16940202
rs16940202 		2 1.000 0.040 16 85980635 intron variant T/C snv 0.15 0.800 1.000 3 2011 2017
dbSNP: rs28374715
rs28374715
CHP1
1 1.000 0.040 15 41271752 intron variant A/G snv 0.25 0.800 1.000 3 2012 2017
dbSNP: rs4380874
rs4380874 		2 1.000 0.040 7 107839870 intergenic variant T/A;C;G snv 0.800 1.000 3 2012 2017
dbSNP: rs483905
rs483905
MAML2
2 1.000 0.040 11 96290263 intron variant G/A snv 0.26 0.800 1.000 3 2012 2017
dbSNP: rs798502
rs798502
GNA12 ; AMZ1
4 1.000 0.040 7 2750246 intron variant A/C;G snv 0.800 1.000 3 2011 2017
dbSNP: rs10797432
rs10797432
LOC100996583
2 1.000 0.040 1 2569899 downstream gene variant C/T snv 0.51 0.800 1.000 2 2012 2017
dbSNP: rs11739663
rs11739663 		1 1.000 0.040 5 593968 intergenic variant T/C snv 0.29 0.800 1.000 2 2011 2012
dbSNP: rs17229285
rs17229285
LOC105373831
2 1.000 0.040 2 198658398 intron variant C/A;T snv 0.800 1.000 2 2012 2015
dbSNP: rs2108225
rs2108225 		2 1.000 0.040 7 107812658 downstream gene variant G/A;T snv 0.810 1.000 2 2009 2018
dbSNP: rs4598195
rs4598195
LOC105375444
1 1.000 0.040 7 107862996 intergenic variant A/C snv 0.34 0.800 1.000 2 2009 2010
dbSNP: rs561722
rs561722
NXPE2
2 1.000 0.040 11 114516108 upstream gene variant C/T snv 0.35 0.800 1.000 2 2012 2015
dbSNP: rs6088765
rs6088765
PROCR ; MMP24OS ; MMP24-AS1-EDEM2
1 1.000 0.040 20 35211477 intron variant T/G snv 0.54 0.800 1.000 2 2012 2015
dbSNP: rs6927022
rs6927022
HLA-DQA1 ; LOC107986589
2 1.000 0.040 6 32644620 non coding transcript exon variant A/G snv 0.42 0.800 1.000 2 2012 2017
dbSNP: rs886774
rs886774 		1 1.000 0.040 7 107854989 regulatory region variant G/A snv 0.67 0.810 1.000 2 2009 2015
dbSNP: rs10010325
rs10010325
TET2 ; TET2-AS1
4 1.000 0.040 4 105185196 intron variant C/A;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10035653
rs10035653
EXOC3 ; EXOC3-AS1
1 1.000 0.040 5 442675 non coding transcript exon variant G/A;T snv 9.1E-02; 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs1016883
rs1016883
PLCL1
1 1.000 0.040 2 198016944 intron variant G/A snv 0.20 0.800 1.000 1 2012 2012
dbSNP: rs10226620
rs10226620
MAFK ; TMEM184A
4 1.000 0.040 7 1541881 3 prime UTR variant T/C snv 0.69 0.010 < 0.001 1 2017 2017
dbSNP: rs10415946
rs10415946
CEACAM6
1 1.000 0.040 19 41755151 intron variant A/G snv 0.39 0.010 1.000 1 2011 2011
dbSNP: rs10416839
rs10416839 		1 1.000 0.040 19 41776424 intron variant G/T snv 0.26 0.010 1.000 1 2011 2011
dbSNP: rs1077773
rs1077773
KCCAT333
2 1.000 0.040 7 17403055 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs10910092
rs10910092
LOC100996583
1 1.000 0.040 1 2570077 downstream gene variant A/G snv 0.52 0.700 1.000 1 2015 2015