NRG4, neuregulin 4, 145957

N. diseases: 71; N. variants: 16
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: rs10851885
rs10851885
0.925 0.120 15 76012162 5 prime UTR variant A/G snv 0.18
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 4 2017 2019
dbSNP: rs11072567
rs11072567
15 76006403 intron variant A/G snv 0.43
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 2 2016 2019
dbSNP: rs10444856
rs10444856
0.925 0.120 15 75940081 3 prime UTR variant T/C snv 0.45
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10444856
rs10444856
0.925 0.120 15 75940081 3 prime UTR variant T/C snv 0.45
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: rs10444856
rs10444856
0.925 0.120 15 75940081 3 prime UTR variant T/C snv 0.45
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: rs10851884
rs10851884
0.925 0.120 15 75997701 intron variant G/A;C;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: rs10851884
rs10851884
0.925 0.120 15 75997701 intron variant G/A;C;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: rs10851884
rs10851884
0.925 0.120 15 75997701 intron variant G/A;C;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs10851885
rs10851885
0.925 0.120 15 76012162 5 prime UTR variant A/G snv 0.18
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: rs10851885
rs10851885
0.925 0.120 15 76012162 5 prime UTR variant A/G snv 0.18
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: rs10851885
rs10851885
0.925 0.120 15 76012162 5 prime UTR variant A/G snv 0.18
Creatinine measurement, serum (procedure)
0.700 1.000 1 2017 2017
dbSNP: rs10851885
rs10851885
0.925 0.120 15 76012162 5 prime UTR variant A/G snv 0.18
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs11072566
rs11072566
0.925 0.120 15 76001630 intron variant A/G snv 0.45
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2017 2017
dbSNP: rs11072566
rs11072566
0.925 0.120 15 76001630 intron variant A/G snv 0.45
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: rs11072566
rs11072566
0.925 0.120 15 76001630 intron variant A/G snv 0.45
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs11072566
rs11072566
0.925 0.120 15 76001630 intron variant A/G snv 0.45
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2012 2012
dbSNP: rs11072566
rs11072566
0.925 0.120 15 76001630 intron variant A/G snv 0.45
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: rs11072567
rs11072567
15 76006403 intron variant A/G snv 0.43
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs11072567
rs11072567
15 76006403 intron variant A/G snv 0.43
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs11072567
rs11072567
15 76006403 intron variant A/G snv 0.43
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs11072567
rs11072567
15 76006403 intron variant A/G snv 0.43
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs11634028
rs11634028
0.925 0.120 15 75983809 intron variant T/A snv 0.14
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: rs11634028
rs11634028
0.925 0.120 15 75983809 intron variant T/A snv 0.14
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: rs11634028
rs11634028
0.925 0.120 15 75983809 intron variant T/A snv 0.14
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs11636220
rs11636220
15 75946727 intron variant A/T snv 0.31
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012