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: rs987525
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		0.800 1.000 3 2009 2012
dbSNP: rs4295627
rs4295627
CCDC26
0.763 0.200 8 129673211 intron variant T/G snv 0.17
CUI: C0017638
Disease: Glioma
Glioma 		0.900 1.000 2 2009 2020
dbSNP: rs4295627
rs4295627
CCDC26
0.763 0.200 8 129673211 intron variant T/G snv 0.17
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms 		0.700 1.000 2 2009 2011
dbSNP: rs7017252
rs7017252
CCDC26
0.925 0.120 8 128938598 intron variant C/T snv 0.32
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		0.800 1.000 1 2009 2017
dbSNP: rs891835
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms 		0.700 1.000 1 2009 2009
dbSNP: rs891835
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17
CUI: C0017638
Disease: Glioma
Glioma 		0.810 1.000 1 2009 2019
dbSNP: rs10098310
rs10098310
CCDC26
8 129601368 intron variant G/A;T snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2011 2011
dbSNP: rs10098310
rs10098310
CCDC26
8 129601368 intron variant G/A;T snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs10956483
rs10956483
CCDC26
8 129559864 intron variant G/A;C snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs10956483
rs10956483
CCDC26
8 129559864 intron variant G/A;C snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2011 2011
dbSNP: rs1991866
rs1991866
CCDC26
8 129611859 intron variant G/A;C snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 2 2012 2017
dbSNP: rs55705857
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02
CUI: C0017638
Disease: Glioma
Glioma 		0.760 1.000 3 2013 2019
dbSNP: rs55705857
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		0.710 1.000 2 2013 2018
dbSNP: rs55705857
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		0.710 1.000 2 2013 2018
dbSNP: rs1991866
rs1991866
CCDC26
8 129611859 intron variant G/A;C snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 2 2014 2017
dbSNP: rs1991866
rs1991866
CCDC26
8 129611859 intron variant G/A;C snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 2 2014 2017
dbSNP: rs10956445
rs10956445
CCDC26
1.000 0.120 8 128775730 intron variant T/C snv 0.20
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		0.700 1.000 1 2014 2014
dbSNP: rs17262815
rs17262815
CCDC26
1.000 0.120 8 129478919 intron variant T/C snv 0.13
CUI: C0848558
Disease: Hypospadias
Hypospadias 		0.700 1.000 1 2014 2014
dbSNP: rs2163950
rs2163950
CCDC26
8 129585339 intron variant C/A snv 9.2E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2014 2014
dbSNP: rs55705857
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms 		0.700 1.000 2 2015 2017
dbSNP: rs13277237
rs13277237
CCDC26
8 129592317 intron variant G/A snv 0.53
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs28540589
rs28540589
CCDC26
8 129104604 intron variant A/T snv 0.19
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs10107630
rs10107630
CCDC26
8 129591389 intron variant C/T snv 0.54
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs10107630
rs10107630
CCDC26
8 129591389 intron variant C/T snv 0.54
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs10107630
rs10107630
CCDC26
8 129591389 intron variant C/T snv 0.54
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016