rs36015961
|
|
G |
0.710 |
CausalMutation |
CLINVAR |
Beta-thalassemia in the Korean population.
|
12144056 |
2002 |
rs36015961
|
|
G |
0.710 |
CausalMutation |
CLINVAR |
Genetic analysis of beta-thalassemia intermedia in Israel: diversity of mechanisms and unpredictability of phenotype.
|
8980256 |
1997 |
rs36015961
|
|
G |
0.710 |
CausalMutation |
CLINVAR |
We describe a novel thalassemic hemoglobinopathy caused by a single nucleotide substitution (CTG-->CCG) at codon 114 resulting in a leucine to proline substitution and designate it beta Durham-NC [beta 114 Leu-->Pro].
|
8111050 |
1994 |
rs36015961
|
|
G |
0.710 |
CausalMutation |
CLINVAR |
Beta-thalassemia alleles and unstable hemoglobin types among Russian pediatric patients.
|
8037185 |
1994 |
rs36015961
|
|
|
0.710 |
GeneticVariation |
BEFREE |
We describe a novel thalassemic hemoglobinopathy caused by a single nucleotide substitution (CTG-->CCG) at codon 114 resulting in a leucine to proline substitution and designate it beta Durham-NC [beta 114 Leu-->Pro].
|
8111050 |
1994 |
rs33944208
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutational Profile of Homozygous β-Thalassemia in Rio de Janeiro, Brazil.
|
28366028 |
2017 |
rs34856846
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Three novel HBB mutations, c.-140C>G (-90 C>G), c.237_256delGGACAACCTCAAGGGCACCT (FS Cd 78/85 -20 bp), and c.315+2T>G (IVS2:2 T>G). Update of the mutational spectrum of β-Thalassemia in Mexican mestizo patients.
|
28603845 |
2017 |
rs63750513
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Cross-Sectional Study for the Detection of Mutations in the Beta-Globin Gene Among Patients with Hemoglobinopathies in the Bengali Population.
|
27828729 |
2017 |
rs33933298
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Report on Ten Years' Experience of Premarital Hemoglobinopathy Screening at a Center in Antalya, Southern Turkey.
|
27207683 |
2016 |
rs33941377
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia Phenotype.
|
27821015 |
2016 |
rs33944208
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The Spectrum of β-Thalassemia Mutations in a Population from the Brazilian Amazon.
|
26372288 |
2016 |
rs33983276
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
|
26635043 |
2016 |
rs33922842
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
High resolution melting analysis: a rapid screening and typing tool for common β-thalassemia mutation in Chinese population.
|
25089872 |
2014 |
rs33944208
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Spectrum of Beta Globin Gene Mutations in Egyptian Children with β-Thalassemia.
|
25408857 |
2014 |
rs35383398
|
|
AC |
0.700 |
CausalMutation |
CLINVAR |
High resolution melting analysis: a rapid screening and typing tool for common β-thalassemia mutation in Chinese population.
|
25089872 |
2014 |
rs35424040
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Hb Knossos: HBB:c.82G>T Associated with HBB:c.315+1G>A Beta Zero Mutation Causes Thalassemia Intermedia.
|
25332589 |
2014 |
rs35456885
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Molecular update of β-thalassemia mutations in the Syrian population: identification of rare β-thalassemia mutations.
|
24828949 |
2014 |
rs35532010
|
|
AG |
0.700 |
CausalMutation |
CLINVAR |
High resolution melting analysis: a rapid screening and typing tool for common β-thalassemia mutation in Chinese population.
|
25089872 |
2014 |
rs33922842
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Hemoglobinopathy: molecular epidemiological characteristics and health effects on Hakka people in the Meizhou region, southern China.
|
23383304 |
2013 |
rs33941377
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Genotyping of beta thalassemia trait by high-resolution DNA melting analysis.
|
24450243 |
2013 |
rs33944208
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The spectrum of β-thalassemia mutations in Gaza Strip, Palestine.
|
23321370 |
2013 |
rs35424040
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
The spectrum of β-thalassemia mutations in Gaza Strip, Palestine.
|
23321370 |
2013 |
rs35619054
|
|
CAGAT |
0.700 |
CausalMutation |
CLINVAR |
Prenatal and newborn screening for hemoglobinopathies.
|
23590658 |
2013 |
rs35662066
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Experience with multiplex ARMS (MARMS)-PCR for the detection of common β-thalassemia mutations in India.
|
22239493 |
2012 |
rs35662066
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Prenatal screening for β-thalassemia major reveals new and rare mutations in the Pakistani population.
|
22392582 |
2012 |