Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs55637647
rs55637647 		1.000 0.120 16 88482856 intron variant C/G snv 0.47
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor 		Neoplasms; Male Urogenital Diseases; Endocrine System Diseases 0.710 1.000 3 2015 2017
dbSNP: rs12232375
rs12232375 		16 88500003 intron variant G/A;C;T snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2016 2019
dbSNP: rs10852622
rs10852622 		16 88490472 intron variant A/G snv 0.35
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs10852622
rs10852622 		16 88490472 intron variant A/G snv 0.35
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs118090537
rs118090537 		16 88493354 intron variant G/A snv 0.14
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs12232375
rs12232375 		16 88500003 intron variant G/A;C;T snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs12232460
rs12232460 		16 88499645 intron variant G/A;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs12445547
rs12445547 		16 88452161 upstream gene variant G/T snv 0.33
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2018 2018
dbSNP: rs12447180
rs12447180 		16 88451314 upstream gene variant T/C snv 0.37
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs12447718
rs12447718 		1.000 0.080 16 88503726 intron variant G/A snv 8.4E-02
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs12597024
rs12597024 		16 88484745 intron variant T/C snv 0.36
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs147032017
rs147032017 		16 88514388 missense variant C/A;T snv 2.0E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2017 2017
dbSNP: rs17175830
rs17175830 		16 88491756 intron variant G/A;C;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs28634651
rs28634651 		16 88486790 intron variant T/A;C;G snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4782369
rs4782369 		16 88465453 intron variant G/A;C snv
CUI: C1629609
Disease: Age at menopause
Age at menopause 		0.700 1.000 1 2019 2019
dbSNP: rs4782371
rs4782371 		1.000 0.040 16 88502423 intron variant T/A;G snv
CUI: C2239222
Disease: Vascular Endothelial Growth Factor Measurement
Vascular Endothelial Growth Factor Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4782371
rs4782371 		1.000 0.040 16 88502423 intron variant T/A;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs59865663
rs59865663 		16 88491904 intron variant G/A snv 0.16
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs7206699
rs7206699 		16 88457407 intron variant T/C snv 0.50
CUI: C0201925
Disease: Calcium measurement
Calcium measurement 		0.700 1.000 1 2018 2018
dbSNP: rs74035509
rs74035509 		16 88500925 intron variant C/T snv 0.10
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs74035509
rs74035509 		16 88500925 intron variant C/T snv 0.10
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs74035509
rs74035509 		16 88500925 intron variant C/T snv 0.10
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs74035509
rs74035509 		16 88500925 intron variant C/T snv 0.10
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs74035509
rs74035509 		16 88500925 intron variant C/T snv 0.10
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs8045833
rs8045833 		16 88509031 intron variant G/A snv 0.32
CUI: C2239222
Disease: Vascular Endothelial Growth Factor Measurement
Vascular Endothelial Growth Factor Measurement 		0.700 1.000 1 2017 2017