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: rs884366
rs884366
CCDC162P
6 109252892 intron variant G/A snv 0.25
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2016 2017
dbSNP: rs117368522
rs117368522
CCDC162P
6 109255740 intron variant G/A snv 5.0E-04
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2017 2017
dbSNP: rs200980971
rs200980971
CCDC162P
6 109261139 intron variant A/-;AA delins
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2017 2017
dbSNP: rs200980971
rs200980971
CCDC162P
6 109261139 intron variant A/-;AA delins
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: rs36052053
rs36052053
CCDC162P
6 109262596 intron variant G/A snv 0.11
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs36052053
rs36052053
CCDC162P
6 109262596 intron variant G/A snv 0.11
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: 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: 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: 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: 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: 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: rs185030778
rs185030778
CCDC162P
6 109277348 intron variant C/T snv 6.3E-03
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs13210693
rs13210693
CCDC162P
1.000 0.040 6 109277761 intron variant G/A snv 0.61
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.800 1.000 1 2011 2011
dbSNP: rs13204927
rs13204927
CCDC162P
6 109281587 intron variant G/A snv 0.39
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
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