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: rs6568571
rs6568571
CCDC162P
6 109292049 intron variant A/C;T snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2017 2017
dbSNP: rs6925716
rs6925716
CCDC162P
6 109276438 intron variant T/C snv 0.61
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs9320282
rs9320282
CCDC162P
6 109298174 intron variant A/G snv 0.63
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs932223
rs932223
CCDC162P
6 109265453 intron variant T/C snv 0.51
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs9372208
rs9372208
CCDC162P
1.000 0.040 6 109274965 intron variant A/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs9372208
rs9372208
CCDC162P
1.000 0.040 6 109274965 intron variant A/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs9374081
rs9374081
CCDC162P
6 109310579 intron variant A/G snv 0.26
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs9386780
rs9386780
CCDC162P
6 109263207 intron variant A/G snv 0.63
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs9386791
rs9386791
CCDC162P
6 109287294 intron variant C/T snv 0.51
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2013 2013
dbSNP: rs9400271
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs9400271
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs9400271
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs9400271
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs9400271
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs9480924
rs9480924
CCDC162P
6 109295867 intron variant T/C snv 0.40
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs9480924
rs9480924
CCDC162P
6 109295867 intron variant T/C snv 0.40
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs9487023
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2017 2017
dbSNP: rs9487023
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs9487023
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs9487023
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2017 2017
dbSNP: rs9487023
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs9487023
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs9487023
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2016 2016
dbSNP: rs9487023
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs9487051
rs9487051
CCDC162P
6 109295876 intron variant A/G snv 0.41
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016