rs281864900
From SNPedia
Merged into | rs80356821 |
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 5.5 | Beta Thalassemia major; Hemoglobin beta-zero; possibly transfusion dependent |
(-;CTTT) | 3 | Beta Thalassemia carrier; Hemoglobin beta-zero mutation; anemia possible |
(CTTT;CTTT) | 0 | common in clinvar |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 5226763 |
Gene | HBB |
is a | snp |
is | mentioned by |
dbSNP | rs281864900 |
dbSNP (classic) | rs281864900 |
ClinGen | rs281864900 |
ebi | rs281864900 |
HLI | rs281864900 |
Exac | rs281864900 |
Gnomad | rs281864900 |
Varsome | rs281864900 |
LitVar | rs281864900 |
Map | rs281864900 |
PheGenI | rs281864900 |
Biobank | rs281864900 |
1000 genomes | rs281864900 |
hgdp | rs281864900 |
ensembl | rs281864900 |
geneview | rs281864900 |
scholar | rs281864900 |
rs281864900 | |
pharmgkb | rs281864900 |
gwascentral | rs281864900 |
openSNP | rs281864900 |
23andMe | rs281864900 |
SNPshot | rs281864900 |
SNPdbe | rs281864900 |
MSV3d | rs281864900 |
GWAS Ctlg | rs281864900 |
Status | Merged into rs80356821 |
Max Magnitude | 5.5 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs281864900(CTTT;CTTT) |
Significance | Pathogenic |
Disease | beta^0^ Thalassemia Alpha Thalassemia |
Variation | info |
Gene | HBB |
CLNDBN | beta^0^ Thalassemia alpha Thalassemia |
Reversed | 1 |
HGVS | NC_000011.9:g.5247993_5247996delAAAG |
CLNSRC | HBVAR OMIM Allelic Variant |
CLNACC | RCV000016673.26, RCV000020328.1, |
[PMID 6826539] Structural analysis of a beta-thalassemia gene found in Taiwan.
[PMID 21250879] Molecular spectrum of α- and β-globin gene mutations detected in the population of Guangxi Zhuang Autonomous Region, People's Republic of China.
[PMID 20113289] Molecular epidemiology investigation of beta-thalassemia in Zhongshan City, Guangdong Province, People's Republic of China.