SLC16A9, solute carrier family 16 member 9, 220963

N. diseases: 12; N. variants: 32
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: rs1171617
rs1171617 		0.925 0.120 10 59707424 intron variant G/A;T snv
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.800 1.000 2 2013 2019
dbSNP: rs1171617
rs1171617 		0.925 0.120 10 59707424 intron variant G/A;T snv
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.800 1.000 2 2013 2019
dbSNP: rs12356193
rs12356193 		0.925 0.120 10 59653595 intron variant A/G snv 0.12
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.800 1.000 1 2009 2009
dbSNP: rs1171618
rs1171618 		0.925 0.120 10 59706183 intron variant T/C snv 0.39
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 2 2010 2013
dbSNP: rs1171618
rs1171618 		0.925 0.120 10 59706183 intron variant T/C snv 0.39
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 2 2010 2013
dbSNP: rs10826342
rs10826342 		0.925 0.120 10 59673534 intron variant T/G snv 0.66
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 2013 2013
dbSNP: rs10826342
rs10826342 		0.925 0.120 10 59673534 intron variant T/G snv 0.66
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11006679
rs11006679 		0.925 0.120 10 59668888 intron variant A/G snv 0.66
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11006679
rs11006679 		0.925 0.120 10 59668888 intron variant A/G snv 0.66
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 2013 2013
dbSNP: rs1171582
rs1171582 		0.925 0.120 10 59734279 intron variant C/T snv 0.34
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1171582
rs1171582 		0.925 0.120 10 59734279 intron variant C/T snv 0.34
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 2013 2013
dbSNP: rs1171606
rs1171606 		0.925 0.120 10 59674761 intron variant G/A;T snv
CUI: C0523446
Disease: Acylcarnitines measurement
Acylcarnitines measurement 		0.700 1.000 1 2015 2015
dbSNP: rs1171606
rs1171606 		0.925 0.120 10 59674761 intron variant G/A;T snv
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 2013 2013
dbSNP: rs1171606
rs1171606 		0.925 0.120 10 59674761 intron variant G/A;T snv
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1171609
rs1171609 		0.925 0.120 10 59719627 intron variant A/G snv 0.54
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 2013 2013
dbSNP: rs1171609
rs1171609 		0.925 0.120 10 59719627 intron variant A/G snv 0.54
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1171610
rs1171610 		0.925 0.120 10 59717939 intron variant C/T snv 0.61
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1171610
rs1171610 		0.925 0.120 10 59717939 intron variant C/T snv 0.61
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 2013 2013
dbSNP: rs1171614
rs1171614 		0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2013 2013
dbSNP: rs1171614
rs1171614 		0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1171614
rs1171614 		0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1171614
rs1171614 		0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1171614
rs1171614 		0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79
CUI: C0523446
Disease: Acylcarnitines measurement
Acylcarnitines measurement 		0.700 1.000 1 2015 2015
dbSNP: rs1171614
rs1171614 		0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1171614
rs1171614 		0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79
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 2013 2013