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: rs12524487
rs12524487 		3 0.925 0.160 6 31386461 upstream gene variant C/T snv 5.9E-02 0.720 1.000 4 2013 2018
dbSNP: rs10919543
rs10919543 		2 1.000 0.080 1 161538827 intron variant A/G snv 0.28 0.720 1.000 2 2013 2016
dbSNP: rs2069837
rs2069837
IL6 ; IL6-AS1
18 0.724 0.520 7 22728408 intron variant A/C;G snv 0.720 1.000 2 2015 2019
dbSNP: rs2099684
rs2099684 		2 1.000 0.080 1 161530340 intron variant A/G snv 0.28 0.710 0.500 2 2017 2018
dbSNP: rs11666543
rs11666543
RPS9
1 1.000 0.080 19 54208113 intron variant A/G snv 0.78 0.710 1.000 1 2015 2015
dbSNP: rs103294
rs103294 		7 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 0.700 1.000 1 2018 2018
dbSNP: rs10921544
rs10921544 		1 1.000 0.080 1 194360431 intergenic variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs113452171
rs113452171
HLA-DQB1-AS1
1 1.000 0.080 6 32658490 upstream gene variant G/T snv 0.700 1.000 1 2013 2013
dbSNP: rs117298325
rs117298325
HLA-B
1 1.000 0.080 6 31312441 intron variant T/C snv 9.6E-03 0.700 1.000 1 2018 2018
dbSNP: rs12047961
rs12047961
LOC105371497
1 1.000 0.080 1 162479619 intergenic variant G/A snv 1.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs12111032
rs12111032
HLA-B
1 1.000 0.080 6 31274414 intron variant A/G snv 0.23 0.700 1.000 1 2015 2015
dbSNP: rs12321966
rs12321966 		1 1.000 0.080 12 8548569 non coding transcript exon variant G/T snv 9.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs12608210
rs12608210 		1 1.000 0.080 18 24913920 intron variant G/A snv 0.31 0.700 1.000 1 2015 2015
dbSNP: rs12980600
rs12980600
RPS9
1 1.000 0.080 19 54203380 intron variant T/A snv 0.79 0.700 1.000 1 2015 2015
dbSNP: rs1383258
rs1383258
HLA-DOB
2 0.925 0.160 6 32815628 intron variant C/T snv 8.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs17133698
rs17133698 		1 1.000 0.080 6 255562 regulatory region variant C/T snv 6.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs1713450
rs1713450
KLHL33
1 1.000 0.080 14 20428086 3 prime UTR variant T/C snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs2322599
rs2322599
PTK2B
1 1.000 0.080 8 27354393 intron variant G/A snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs2457837
rs2457837
FRMD4A
1 1.000 0.080 10 14009457 intron variant C/T snv 0.38 0.700 1.000 1 2015 2015
dbSNP: rs2736173
rs2736173
PRRC2A ; SNORA38
1 1.000 0.080 6 31621958 intron variant C/T snv 1.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs28399987
rs28399987
MSH5 ; SAPCD1 ; MSH5-SAPCD1
1 1.000 0.080 6 31762974 3 prime UTR variant G/A snv 6.5E-03 0.700 1.000 1 2015 2015
dbSNP: rs3869115
rs3869115 		1 1.000 0.080 6 31236917 intergenic variant C/G snv 9.5E-02 0.700 1.000 1 2015 2015
dbSNP: rs41267090
rs41267090
CYP21A2 ; EHMT2 ; SLC44A4 ; EHMT2-AS1 ; LOC107986588
1 1.000 0.080 6 31880663 non coding transcript exon variant A/G;T snv 8.0E-06; 4.5E-02 0.700 1.000 1 2015 2015
dbSNP: rs4410768
rs4410768
CDSN ; PSORS1C1
1 1.000 0.080 6 31121931 intron variant A/G snv 1.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs4463283
rs4463283 		1 1.000 0.080 6 29097215 upstream gene variant C/A;T snv 8.1E-02 0.700 1.000 1 2015 2015