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: rs11327184
rs11327184
CCDC26
8 129592027 intron variant C/- delins 0.40
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs11783015
rs11783015
CCDC26
1.000 0.040 8 128682763 intron variant T/C snv 0.23
CUI: C0013595
Disease: Eczema
Eczema 		0.700 1.000 1 2019 2019
dbSNP: rs12548560
rs12548560
CCDC26
8 129094808 intron variant A/G snv 0.41
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs13277237
rs13277237
CCDC26
8 129592317 intron variant G/A snv 0.53
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2017 2017
dbSNP: rs13277237
rs13277237
CCDC26
8 129592317 intron variant G/A snv 0.53
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2017 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: rs13277237
rs13277237
CCDC26
8 129592317 intron variant G/A snv 0.53
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs138628047
rs138628047
CCDC26
8 129666460 intron variant T/C;G snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs138628047
rs138628047
CCDC26
8 129666460 intron variant T/C;G snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs1433578
rs1433578
CCDC26
8 129588843 intron variant T/C snv 9.1E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2018 2018
dbSNP: rs1583333
rs1583333
CCDC26
0.925 0.040 8 129602653 intron variant C/A snv 0.18
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs1583333
rs1583333
CCDC26
0.925 0.040 8 129602653 intron variant C/A snv 0.18
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs17242358
rs17242358
CCDC26 ; LINC00976
1.000 8 128952627 intron variant G/A snv 0.14
CUI: C4021813
Disease: Oral cleft
Oral cleft 		0.700 1.000 1 2017 2017
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: rs1982094
rs1982094
CCDC26
8 129612570 intron variant C/T snv 4.8E-02
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1982094
rs1982094
CCDC26
8 129612570 intron variant C/T snv 4.8E-02
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs1982094
rs1982094
CCDC26
8 129612570 intron variant C/T snv 4.8E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs1982094
rs1982094
CCDC26
8 129612570 intron variant C/T snv 4.8E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs1982094
rs1982094
CCDC26
8 129612570 intron variant C/T snv 4.8E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
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: rs2395906
rs2395906
CCDC26
8 129598547 intron variant G/A;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2719209
rs2719209
CCDC26
8 129415405 intron variant C/A snv 0.17
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
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: rs28665337
rs28665337
CCDC26
1.000 0.120 8 129181858 intron variant C/A;T snv
CUI: C0023485
Disease: Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma 		0.700 1.000 1 2018 2018
dbSNP: rs35389394
rs35389394
CCDC26
8 129609008 intron variant C/T snv 0.56
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2018 2018