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: 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: 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: 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: rs12529733
rs12529733
CCDC162P
6 109332929 intron variant T/C snv 0.54
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
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: 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: rs9400273
rs9400273
CCDC162P
6 109311596 intron variant A/G snv 0.40
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2017 2018
dbSNP: rs1008084
rs1008084
CCDC162P
6 109305762 intron variant G/A snv 0.40
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2012 2012
dbSNP: rs11966072
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2010 2010
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: 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: 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: 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: 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: 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: rs11966072
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2010 2010
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: 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: 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: rs9374080
rs9374080
CCDC162P
6 109295217 intron variant T/C snv 0.40
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.800 1.000 2 2009 2017
dbSNP: rs11966072
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2010 2010
dbSNP: rs13191948
rs13191948
CCDC162P
6 109313396 intron variant C/T snv 0.40
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2018 2018
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: 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