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: rs117491755
rs117491755
ASTN2
1 1.000 0.080 9 116881377 intron variant A/C snv 2.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs149014830
rs149014830 		1 1.000 0.080 5 121540642 intergenic variant C/A;G snv 1.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs17036170
rs17036170
PPARG
2 1.000 0.080 3 12288912 5 prime UTR variant G/A snv 1.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs191153876
rs191153876
CCDC14
1 1.000 0.080 3 123918335 intron variant A/T snv 1.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs2240395
rs2240395
TBXAS1
1 1.000 0.080 7 140018347 intron variant C/G;T snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs28521457
rs28521457
LRBA
1 1.000 0.080 4 150759175 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs114811931
rs114811931 		1 1.000 0.080 5 161257724 intergenic variant T/C snv 1.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs1495741
rs1495741 		9 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs10937275
rs10937275
ST6GAL1
1 1.000 0.080 3 186933001 intron variant A/G snv 0.88 0.800 1.000 1 2009 2009
dbSNP: rs6694270
rs6694270 		1 1.000 0.080 1 18793883 intergenic variant A/G snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs2205986
rs2205986
SYT14
2 0.925 0.160 1 209942767 intron variant G/A snv 0.92 0.700 1.000 1 2018 2018
dbSNP: rs11012476
rs11012476
NEBL
3 0.925 0.120 10 21003994 intron variant C/T snv 3.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs10812428
rs10812428 		1 1.000 0.080 9 26614849 intergenic variant C/T snv 0.40 0.800 1.000 1 2009 2009
dbSNP: rs116606120
rs116606120 		1 1.000 0.080 5 28665845 intron variant T/A snv 1.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs2523822
rs2523822 		1 1.000 0.080 6 29860883 intron variant A/G snv 0.26 0.800 1.000 1 2011 2011
dbSNP: rs114577328
rs114577328
HLA-A
2 1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs2395029
rs2395029
HCP5
12 0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 0.800 1.000 2 2009 2019
dbSNP: rs3129900
rs3129900
TSBP1 ; TSBP1-AS1
3 0.882 0.200 6 32338202 intron variant G/T snv 0.83 0.800 1.000 1 2010 2010
dbSNP: rs9274407
rs9274407
HLA-DQB1
3 0.925 0.120 6 32665055 missense variant A/C;T snv 0.77 0.800 1.000 1 2011 2011
dbSNP: rs6582630
rs6582630 		1 1.000 0.080 12 38349706 intergenic variant G/A snv 0.62 0.800 1.000 1 2009 2009
dbSNP: rs6139258
rs6139258
RNF24
2 1.000 0.080 20 3977969 intron variant T/C snv 3.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs10404821
rs10404821
C19orf81
1 1.000 0.080 19 50657831 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs72631567
rs72631567 		2 1.000 0.080 2 5092045 intergenic variant A/G snv 4.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs186920977
rs186920977 		1 1.000 0.080 2 56422795 intergenic variant G/A snv 1.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs61858823
rs61858823 		1 1.000 0.080 10 65095495 intergenic variant G/A snv 1.3E-02 0.700 1.000 1 2017 2017