Source: GWASCAT

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: rs533614130
rs533614130
FAM234A
16 236001 intron variant A/G snv 3.4E-04
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
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: rs76792961
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs13339636
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2017 2017
dbSNP: rs13339636
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2017 2017
dbSNP: rs13339636
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2017 2017
dbSNP: rs13339636
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2013 2013
dbSNP: rs13339636
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.800 1.000 1 2013 2017
dbSNP: rs13331259
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 2 2019 2019
dbSNP: rs13331259
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2019 2019
dbSNP: rs13331259
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs13331259
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs13331259
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs13331259
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2019 2019