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rs121909825

From SNPedia

Merged intors35553496
Orientationminus
Stabilizedminus
Make rs121909825(A;A)
Make rs121909825(A;C)
Make rs121909825(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226630
GeneHBB
is asnp
is mentioned by
dbSNPrs121909825
ebirs121909825
HLIrs121909825
Exacrs121909825
Varsomers121909825
Maprs121909825
PheGenIrs121909825
hapmaprs121909825
1000 genomesrs121909825
hgdprs121909825
ensemblrs121909825
gopubmedrs121909825
geneviewrs121909825
scholarrs121909825
googlers121909825
pharmgkbrs121909825
gwascentralrs121909825
openSNPrs121909825
23andMers121909825
23andMe allrs121909825
SNP Nexus

SNPshotrs121909825
SNPdbers121909825
MSV3drs121909825
GWAS Ctlgrs121909825
StatusMerged into rs35553496
Max Magnitude
OMIM141900
Desc
Variant0400
Relatedalso

[PMID 1709134] The linkage of Hb Valletta [alpha 2 beta 287(f3)Thr----Pro] and Hb F-Malta-I [alpha 2G gamma 2117(G19)His----Arg] in the Maltese population.


[PMID 9028827] Hb Valletta [beta 87(F3)Thr-->Pro] due to an A-->C substitution at codon 87 in a Calabrian family with alpha-thalassemia.


[PMID 17145605] Analysis of delta-globin gene alleles in the Sicilian population: identification of five new mutations.


[PMID 21194254] First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA(2)-NYU in Iran.