Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1059362
rs1059362
HLA-DRB1
6 32580773 synonymous variant G/A snv 7.2E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs113399573
rs113399573
HLA-DRB1
6 32591382 upstream gene variant C/T snv 0.23
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs116763083
rs116763083
HLA-DRB1
6 32602155 intergenic variant T/A snv 4.4E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2308765
rs2308765
HLA-DRB1
6 32581757 missense variant A/C;G;T snv 7.6E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2012 2012
dbSNP: rs2647062
rs2647062
HLA-DRB1
6 32602640 intergenic variant A/C snv 0.13
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2647074
rs2647074
HLA-DRB1
6 32606583 intergenic variant C/T snv 0.30
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2647074
rs2647074
HLA-DRB1
6 32606583 intergenic variant C/T snv 0.30
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2760995
rs2760995
HLA-DRB1
6 32606581 intergenic variant G/A snv 0.20
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria 		0.700 1.000 1 2019 2019
dbSNP: rs28366255
rs28366255
HLA-DRB1
6 32591705 upstream gene variant C/A;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs28366266
rs28366266
HLA-DRB1
6 32591976 upstream gene variant T/C snv 0.12
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		0.700 1.000 1 2018 2018
dbSNP: rs9256938
rs9256938
HLA-DRB1
6 32579417 intron variant C/A;G snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs9270493
rs9270493
HLA-DRB1
6 32591333 upstream gene variant T/C snv 0.25
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs9270637
rs9270637
HLA-DRB1
6 32597873 intergenic variant A/C;G snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs9270891
rs9270891
HLA-DRB1
6 32604051 intergenic variant T/G snv 0.60
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs113520250
rs113520250
HLA-DRB1
1.000 0.040 6 32587108 intron variant C/T snv 0.26
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		0.700 1.000 1 2012 2012
dbSNP: rs115673262
rs115673262
HLA-DRB1
1.000 0.040 6 32604965 intergenic variant C/G snv
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		0.700 1.000 1 2012 2012
dbSNP: rs115736757
rs115736757
HLA-DRB1
1.000 0.040 6 32607947 intergenic variant T/C snv 4.7E-02
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		0.700 1.000 1 2012 2012
dbSNP: rs116119619
rs116119619
HLA-DRB1
1.000 0.040 6 32607948 intergenic variant G/A snv 4.7E-02
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		0.700 1.000 1 2012 2012
dbSNP: rs11753207
rs11753207
HLA-DRB1
1.000 0.040 6 32584671 intron variant A/C snv 0.12
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs11753207
rs11753207
HLA-DRB1
1.000 0.040 6 32584671 intron variant A/C snv 0.12
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs13191764
rs13191764
HLA-DRB1
1.000 0.040 6 32602333 intergenic variant T/A snv 4.8E-02
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		0.700 1.000 1 2012 2012
dbSNP: rs142790902
rs142790902
HLA-DRB1
1.000 0.040 6 32582137 intron variant T/C snv 6.0E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs142790902
rs142790902
HLA-DRB1
1.000 0.040 6 32582137 intron variant T/C snv 6.0E-02
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs144453041
rs144453041
HLA-DRB1
1.000 0.040 6 32605248 intergenic variant A/G snv
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		0.700 1.000 1 2012 2012
dbSNP: rs144660248
rs144660248
HLA-DRB1
1.000 0.040 6 32583926 intron variant G/T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017