MIXL1, Mix paired-like homeobox, 83881

N. diseases: 33; N. variants: 1
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs368705607
rs368705607 		0.882 0.120 1 226225766 missense variant T/C;G snv 2.8E-05; 4.0E-06
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs368705607
rs368705607 		0.882 0.120 1 226225766 missense variant T/C;G snv 2.8E-05; 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs368705607
rs368705607 		0.882 0.120 1 226225766 missense variant T/C;G snv 2.8E-05; 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2015 2015
dbSNP: rs368705607
rs368705607 		0.882 0.120 1 226225766 missense variant T/C;G snv 2.8E-05; 4.0E-06
CUI: C0220810
Disease: Congenital defects
Congenital defects 		0.010 1.000 1 2016 2016
dbSNP: rs368705607
rs368705607 		0.882 0.120 1 226225766 missense variant T/C;G snv 2.8E-05; 4.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs368705607
rs368705607 		0.882 0.120 1 226225766 missense variant T/C;G snv 2.8E-05; 4.0E-06
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 < 0.001 1 2015 2015
dbSNP: rs368705607
rs368705607 		0.882 0.120 1 226225766 missense variant T/C;G snv 2.8E-05; 4.0E-06
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities 0.010 1.000 1 2016 2016