rs121912734
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 Associated with Darier Disease and Hailey-Hailey Disease.
|
28035777 |
2017 |
rs121912734
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Three-base deletion mutation c.120_122delGTT in ATP2A2 leads to the unique phenotype of comedonal Darier disease.
|
19995371 |
2010 |
rs121912734
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes.
|
10441325 |
1999 |
rs121912734
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class.
|
10441324 |
1999 |
rs121912734
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Spectrum of novel ATP2A2 mutations in patients with Darier's disease.
|
10441323 |
1999 |
rs121912734
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease.
|
10080178 |
1999 |
rs121912738
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 Associated with Darier Disease and Hailey-Hailey Disease.
|
28035777 |
2017 |
rs121912738
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Three-base deletion mutation c.120_122delGTT in ATP2A2 leads to the unique phenotype of comedonal Darier disease.
|
19995371 |
2010 |
rs121912738
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class.
|
10441324 |
1999 |
rs121912738
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease.
|
10080178 |
1999 |
rs121912738
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes.
|
10441325 |
1999 |
rs121912738
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Spectrum of novel ATP2A2 mutations in patients with Darier's disease.
|
10441323 |
1999 |
rs28929478
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs121912732
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 Associated with Darier Disease and Hailey-Hailey Disease.
|
28035777 |
2017 |
rs121912733
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 Associated with Darier Disease and Hailey-Hailey Disease.
|
28035777 |
2017 |
rs121912736
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 Associated with Darier Disease and Hailey-Hailey Disease.
|
28035777 |
2017 |
rs121912732
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Three-base deletion mutation c.120_122delGTT in ATP2A2 leads to the unique phenotype of comedonal Darier disease.
|
19995371 |
2010 |
rs121912733
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Three-base deletion mutation c.120_122delGTT in ATP2A2 leads to the unique phenotype of comedonal Darier disease.
|
19995371 |
2010 |
rs121912736
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Three-base deletion mutation c.120_122delGTT in ATP2A2 leads to the unique phenotype of comedonal Darier disease.
|
19995371 |
2010 |
rs121912732
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Spectrum of novel ATP2A2 mutations in patients with Darier's disease.
|
10441323 |
1999 |
rs121912732
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes.
|
10441325 |
1999 |
rs121912732
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class.
|
10441324 |
1999 |
rs121912732
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease.
|
10080178 |
1999 |
rs121912733
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Spectrum of novel ATP2A2 mutations in patients with Darier's disease.
|
10441323 |
1999 |
rs121912733
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease.
|
10080178 |
1999 |