TYR, tyrosinase, 7299

N. diseases: 281; N. variants: 121
Disease: Albinism ×
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: rs1126809
rs1126809 		0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.710 1.000 1 2013 2013
dbSNP: rs28940876
rs28940876 		0.827 0.160 11 89178195 missense variant C/T snv 8.4E-05 1.7E-04
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.700 1.000 1 1990 1990
dbSNP: rs749979474
rs749979474 		1.000 0.160 11 89284852 missense variant C/T snv 1.6E-05 4.2E-05
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.700 1.000 1 2003 2003
dbSNP: rs104894313
rs104894313 		0.807 0.160 11 89284805 missense variant C/T snv 3.8E-03; 4.0E-06 3.7E-03
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs121908011
rs121908011 		0.827 0.160 11 89227933 missense variant G/A snv 9.2E-05 3.5E-05
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs28940877
rs28940877 		0.807 0.200 11 89178218 missense variant T/C snv 4.0E-06 2.1E-05
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs28940881
rs28940881 		0.776 0.200 11 89177954 start lost A/G snv 6.4E-05 5.6E-05
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs376823382
rs376823382 		0.827 0.200 11 89284940 missense variant A/G snv 1.9E-04 2.2E-04
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs61753253
rs61753253 		0.925 0.160 11 89178278 missense variant G/A snv 5.2E-05 8.4E-05
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs61754381
rs61754381 		0.790 0.200 11 89227816 splice region variant T/A;C snv 9.5E-04; 8.0E-06
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs62645904
rs62645904 		0.827 0.160 11 89191214 stop gained C/A;T snv 1.9E-04
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs104894314
rs104894314 		0.790 0.160 11 89191205 missense variant G/A;T snv 8.0E-06; 9.2E-05
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.010 1.000 1 2016 2016
dbSNP: rs61753185
rs61753185 		0.882 0.160 11 89178183 missense variant G/A snv 8.4E-05 5.6E-05
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017
dbSNP: rs61754388
rs61754388 		0.827 0.160 11 89227904 missense variant C/A snv 3.4E-04 5.0E-04
CUI: C0001916
Disease: Albinism
Albinism 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018