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rs121909821

From SNPedia

Merged intors33930385
Orientationminus
Stabilizedminus
Make rs121909821(G;G)
Make rs121909821(G;T)
Make rs121909821(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226642
GeneHBB
is asnp
is mentioned by
dbSNPrs121909821
ebirs121909821
HLIrs121909821
Exacrs121909821
Varsomers121909821
Maprs121909821
PheGenIrs121909821
hapmaprs121909821
1000 genomesrs121909821
hgdprs121909821
ensemblrs121909821
gopubmedrs121909821
geneviewrs121909821
scholarrs121909821
googlers121909821
pharmgkbrs121909821
gwascentralrs121909821
openSNPrs121909821
23andMers121909821
23andMe allrs121909821
SNP Nexus

SNPshotrs121909821
SNPdbers121909821
MSV3drs121909821
GWAS Ctlgrs121909821
StatusMerged into rs33930385
Max Magnitude
OMIM141900
Desc
Variant0277
Relatedalso
OMIM141900
Desc
Variant0432
Relatedalso

[PMID 5129589] Hemoglobin Ta-Li: 83 Gly leads to Cys.


[PMID 11838022] Characterization of the elusive disulfide bridge forming human Hb variant: Hb Ta-Li beta83 (EF7)Gly --> Cys by electrospray mass spectrometry.


[PMID 8454474] Hb Muskegon [beta 83(EF7)Gly-->Arg]: a new variant found in a family from the U.S.