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: rs1074532
rs1074532 		1 1.000 0.080 4 65791342 intergenic variant A/G snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs11218708
rs11218708 		1 1.000 0.080 11 122601355 regulatory region variant G/A snv 0.19 0.710 1.000 1 2018 2018
dbSNP: rs17315309
rs17315309
ST18
1 1.000 0.080 8 52295127 intron variant A/G;T snv 0.12 0.010 1.000 1 2019 2019
dbSNP: rs2523647
rs2523647
MICB-DT
1 1.000 0.080 6 31482001 intron variant A/G snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs28483633
rs28483633 		1 1.000 0.080 6 32657097 upstream gene variant C/A snv 2.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs482759
rs482759 		1 1.000 0.080 6 32227240 upstream gene variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1051336
rs1051336
HLA-DRA
2 0.925 0.120 6 32444815 3 prime UTR variant G/A;C snv 0.15 0.010 1.000 1 2018 2018
dbSNP: rs1980495
rs1980495
TSBP1-AS1
2 0.925 0.160 6 32379017 intron variant A/C snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs2516424
rs2516424
MICB-DT
2 0.925 0.160 6 31480538 non coding transcript exon variant A/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs7454108
rs7454108 		2 0.925 0.120 6 32713706 upstream gene variant T/C snv 9.1E-02 0.710 1.000 1 2018 2018
dbSNP: rs12660382
rs12660382
HCP5
3 0.882 0.200 6 31475546 intron variant C/T snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs2244839
rs2244839
HCP5 ; HCG26
3 0.882 0.200 6 31470591 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2246618
rs2246618
MICB
3 0.882 0.160 6 31511209 upstream gene variant C/T snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs2395163
rs2395163 		3 0.882 0.160 6 32420032 intergenic variant T/C snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs2395488
rs2395488
HCP5
3 0.882 0.160 6 31478132 non coding transcript exon variant A/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs3763309
rs3763309
BTNL2 ; TSBP1-AS1
3 0.882 0.160 6 32408196 upstream gene variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3916765
rs3916765
LOC102725019
3 0.882 0.200 6 32717773 upstream gene variant G/A snv 8.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs6941112
rs6941112
CYP21A2 ; STK19
3 0.882 0.120 6 31978837 intron variant G/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs70993900
rs70993900 		3 0.882 0.080 6 32618381 intergenic variant C/- delins 4.8E-02 0.710 1.000 1 2019 2019
dbSNP: rs9275184
rs9275184 		3 0.882 0.200 6 32686937 regulatory region variant T/C snv 9.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs9275390
rs9275390 		3 0.882 0.120 6 32701379 downstream gene variant T/C snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs3892710
rs3892710 		4 0.851 0.240 6 32715085 upstream gene variant C/T snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs443198
rs443198
NOTCH4
4 0.851 0.200 6 32222629 synonymous variant A/G snv 0.38 0.39 0.700 1.000 1 2012 2012
dbSNP: rs9268542
rs9268542 		4 0.851 0.280 6 32416944 intergenic variant A/G snv 0.35 0.700 1.000 1 2012 2012
dbSNP: rs2395157
rs2395157
TSBP1-AS1
5 0.827 0.240 6 32380368 intron variant A/G snv 0.24 0.700 1.000 1 2012 2012