Source: CURATED ×
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: rs4760
rs4760 		1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs2302524
rs2302524 		1.000 0.040 19 43652320 missense variant T/C snv 0.16 0.17
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs36229204
rs36229204 		19 43671830 upstream gene variant C/T snv 3.0E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4251884
rs4251884 		19 43655632 intron variant G/A snv 3.7E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4251884
rs4251884 		19 43655632 intron variant G/A snv 3.7E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4760
rs4760 		1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs4760
rs4760 		1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11
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: rs4760
rs4760 		1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs4760
rs4760 		1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs4760
rs4760 		1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs4760
rs4760 		1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016