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: rs1990760
rs1990760
IFIH1
33 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 0.710 1.000 2 2010 2016
dbSNP: rs10071761
rs10071761 		2 0.925 0.080 5 40415509 intron variant T/C snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs10905875
rs10905875
LOC101928080
2 0.925 0.080 10 6131814 intergenic variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs11299600
rs11299600 		2 0.925 0.080 8 128192327 regulatory region variant A/- delins 0.29 0.700 1.000 1 2016 2016
dbSNP: rs116041786
rs116041786
HLA-DQA1
2 0.925 0.080 6 32634619 intron variant C/T snv 0.700 1.000 1 2016 2016
dbSNP: rs12257092
rs12257092 		2 0.925 0.080 10 89023070 intergenic variant A/T snv 0.27 0.700 1.000 1 2016 2016
dbSNP: rs1244181
rs1244181
GATA3
2 0.925 0.080 10 8049414 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs12967678
rs12967678
PTPN2
2 0.925 0.080 18 12805389 intron variant G/A snv 8.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs146583707
rs146583707 		2 0.925 0.080 4 122571262 intergenic variant T/A snv 0.20 0.700 1.000 1 2016 2016
dbSNP: rs16862780
rs16862780
LINC01991
3 0.925 0.080 3 187970052 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2136613
rs2136613
EGR2
2 0.925 0.080 10 62834404 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs2210913
rs2210913
FCRL3
2 0.925 0.080 1 157699203 intron variant C/T snv 0.56 0.700 1.000 1 2016 2016
dbSNP: rs34069391
rs34069391
CLEC16A
2 0.925 0.080 16 11067358 intron variant T/- delins 0.700 1.000 1 2016 2016
dbSNP: rs4565870
rs4565870 		2 0.925 0.080 11 46328319 upstream gene variant T/C snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs67257959
rs67257959 		2 0.925 0.080 19 17047335 upstream gene variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs7773987
rs7773987
AHI1
2 0.925 0.080 6 135386348 intron variant C/T snv 0.60 0.700 1.000 1 2016 2016
dbSNP: rs80168506
rs80168506
LOC107985981
2 0.925 0.080 2 213196729 intergenic variant A/G snv 5.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs8071789
rs8071789
IKZF3
2 0.925 0.080 17 39850080 intron variant C/T snv 0.47 0.700 1.000 1 2016 2016
dbSNP: rs9831894
rs9831894
CD86
3 0.882 0.120 3 122081640 intron variant A/C snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs2069849
rs2069849
IL6
3 0.882 0.120 7 22731537 missense variant C/G;T snv 4.4E-02 0.010 1.000 1 2008 2008
dbSNP: rs35667974
rs35667974
IFIH1
9 0.776 0.280 2 162268127 missense variant T/C snv 1.1E-02 1.2E-02 0.010 1.000 1 2016 2016
dbSNP: rs373643598
rs373643598
IL12RB1
1 1.000 19 18072286 stop gained G/A snv 1.2E-05 0.010 < 0.001 1 2011 2011
dbSNP: rs747650808
rs747650808
AMBRA1
1 1.000 11 46410310 missense variant C/T snv 1.2E-05 0.010 1.000 1 2016 2016