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: rs2524079
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.800 1.000 4 2011 2019
dbSNP: rs2524079
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 2 2011 2017
dbSNP: rs2853946
rs2853946
HLA-B
6 31279426 intron variant A/G;T snv 0.37
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 2 2014 2019
dbSNP: rs10569394
rs10569394
HLA-B ; HLA-C
6 31272468 intron variant -/TC delins
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs111721712
rs111721712
HLA-B
6 31347630 intron variant -/T delins 0.55
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1140404
rs1140404
HLA-B ; MIR6891
6 31356750 missense variant T/C;G snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs114208039
rs114208039
HLA-B ; HLA-C
6 31273862 intron variant A/G snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2018 2018
dbSNP: rs114208039
rs114208039
HLA-B ; HLA-C
6 31273862 intron variant A/G snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2018 2018
dbSNP: rs114398276
rs114398276
HLA-B
6 31279046 intron variant A/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2018 2018
dbSNP: rs114584519
rs114584519
HLA-B
6 31345371 intron variant A/T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2018 2018
dbSNP: rs114811870
rs114811870
HLA-B ; MIR6891
6 31357161 5 prime UTR variant C/T snv 4.2E-02 8.2E-02
CUI: C0202075
Disease: 17 Hydroxyprogesterone measurement
17 Hydroxyprogesterone measurement 		0.700 1.000 1 2019 2019
dbSNP: rs115681968
rs115681968
HLA-B ; LOC112267902
6 31304776 intron variant G/A snv
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2018 2018
dbSNP: rs115845232
rs115845232
HLA-B ; LOC112267902
6 31304484 intron variant C/T snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs115845232
rs115845232
HLA-B ; LOC112267902
6 31304484 intron variant C/T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs115845232
rs115845232
HLA-B ; LOC112267902
6 31304484 intron variant C/T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs116438126
rs116438126
HLA-B
6 31348683 intron variant C/T snv 9.0E-03
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs116576188
rs116576188
HLA-B
6 31328592 intron variant A/C snv 1.2E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs116685461
rs116685461
HLA-B
6 31347735 intron variant G/A snv 0.14
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1625792
rs1625792
HLA-B
6 31338643 intron variant G/A snv 8.8E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs1634738
rs1634738
HLA-B
6 31316290 intron variant G/A;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17199328
rs17199328
HLA-B
6 31354618 non coding transcript exon variant A/C;G;T snv 4.0E-06; 9.8E-02
CUI: C0019360
Disease: Herpes zoster disease
Herpes zoster disease 		0.700 1.000 1 2019 2019
dbSNP: rs2308575
rs2308575
HLA-B ; HLA-C
6 31271280 stop lost C/G;T snv 2.2E-05; 0.25
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2394982
rs2394982
HLA-B
6 31345253 intron variant C/T snv 0.20
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs2523625
rs2523625
HLA-B
6 31347871 intron variant A/G snv 0.32
CUI: C0518026
Disease: body fat percentage (physical finding)
body fat percentage (physical finding) 		0.700 1.000 1 2019 2019
dbSNP: rs2524043
rs2524043
HLA-B
6 31289235 intron variant A/G snv 0.10
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012