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: rs11866328
rs11866328
GRIN2A
3 0.925 0.120 16 9768699 intron variant G/T snv 0.38 0.810 1.000 1 2011 2011
dbSNP: rs3130542
rs3130542 		8 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 0.810 1.000 1 2013 2013
dbSNP: rs1419881
rs1419881
TCF19
4 0.851 0.280 6 31162816 3 prime UTR variant G/A snv 0.50 0.800 1.000 1 2013 2013
dbSNP: rs652888
rs652888
CYP21A2 ; EHMT2 ; EHMT2-AS1 ; LOC107986588
10 0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 0.800 1.000 1 2013 2013
dbSNP: rs7756516
rs7756516
HLA-DQB2
4 0.851 0.280 6 32756140 3 prime UTR variant C/T snv 0.49 0.710 1.000 1 2014 2014
dbSNP: rs10214910
rs10214910
HLA-DPA1
1 1.000 0.080 6 33069898 intron variant C/A snv 0.23 0.32 0.700 1.000 1 2013 2013
dbSNP: rs10243492
rs10243492 		1 1.000 0.080 7 32780825 intergenic variant A/G snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs10272859
rs10272859
CDK14
4 0.925 0.120 7 90689160 intron variant G/C snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs1042190
rs1042190
HLA-DPA1
1 1.000 0.080 6 33069222 missense variant T/C snv 0.24 0.28 0.700 1.000 1 2013 2013
dbSNP: rs1042544
rs1042544
HLA-DPB1
2 0.925 0.200 6 33086680 3 prime UTR variant A/G snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs11089620
rs11089620
UBE2L3
1 1.000 0.080 22 21568167 non coding transcript exon variant C/G snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs1110446
rs1110446
TRIM31
2 0.925 0.120 6 30103160 3 prime UTR variant C/T snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs1126542
rs1126542
HLA-DPA1
1 1.000 0.080 6 33069647 missense variant T/A;C;G snv 0.24 0.28 0.700 1.000 1 2013 2013
dbSNP: rs1126769
rs1126769
HLA-DPA1
1 1.000 0.080 6 33068658 missense variant T/G snv 0.24 0.29 0.700 1.000 1 2013 2013
dbSNP: rs11638027
rs11638027 		1 1.000 0.080 15 90302268 intron variant G/T snv 9.9E-02 0.700 1.000 1 2013 2013
dbSNP: rs11752643
rs11752643 		2 0.925 0.120 6 32701596 downstream gene variant C/T snv 2.3E-02 0.700 1.000 1 2011 2011
dbSNP: rs12484550
rs12484550
UBE2L3
1 1.000 0.080 22 21587626 intron variant C/T snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs1260326
rs1260326
GCKR
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2011 2011
dbSNP: rs12649554
rs12649554 		1 1.000 0.080 4 100975519 regulatory region variant T/C snv 0.65 0.700 1.000 1 2011 2011
dbSNP: rs1265115
rs1265115
CCHCR1
5 0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs12663103
rs12663103
GPSM3
7 0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 0.700 1.000 1 2011 2011
dbSNP: rs13199787
rs13199787 		2 0.925 0.200 6 32737499 upstream gene variant C/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs13213149
rs13213149
HLA-DPA1
1 1.000 0.080 6 33071909 intron variant T/C snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs1383265
rs1383265 		2 0.925 0.200 6 32772111 intergenic variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs1431400
rs1431400
HLA-DPA1
1 1.000 0.080 6 33073399 intron variant C/T snv 0.29 0.700 1.000 1 2013 2013