MAPK6, mitogen-activated protein kinase 6, 5597

N. diseases: 40; N. variants: 4
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: rs16964657
rs16964657 		1.000 0.040 15 51982216 intron variant C/T snv 7.1E-02
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia 		Male Urogenital Diseases 0.700 1.000 1 2012 2012
dbSNP: rs16964720
rs16964720 		0.925 0.040 15 52059716 intron variant C/G snv 9.2E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs16964720
rs16964720 		0.925 0.040 15 52059716 intron variant C/G snv 9.2E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs62015197
rs62015197 		0.925 0.120 15 52048569 intron variant A/G snv 3.3E-02
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2015 2015
dbSNP: rs62015197
rs62015197 		0.925 0.120 15 52048569 intron variant A/G snv 3.3E-02
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2015 2015
dbSNP: rs62015197
rs62015197 		0.925 0.120 15 52048569 intron variant A/G snv 3.3E-02
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2015 2015
dbSNP: rs35697691
rs35697691 		15 52061301 missense variant C/G snv 5.8E-02 5.9E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs35697691
rs35697691 		15 52061301 missense variant C/G snv 5.8E-02 5.9E-02
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.010 1.000 1 2017 2017
dbSNP: rs35697691
rs35697691 		15 52061301 missense variant C/G snv 5.8E-02 5.9E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2017 2017