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rs121909811

From SNPedia

Merged intors33985847
Orientationminus
Stabilizedminus
Make rs121909811(A;A)
Make rs121909811(A;C)
Make rs121909811(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226662
GeneHBB
is asnp
is mentioned by
dbSNPrs121909811
ebirs121909811
HLIrs121909811
Exacrs121909811
Varsomers121909811
Maprs121909811
PheGenIrs121909811
hapmaprs121909811
1000 genomesrs121909811
hgdprs121909811
ensemblrs121909811
gopubmedrs121909811
geneviewrs121909811
scholarrs121909811
googlers121909811
pharmgkbrs121909811
gwascentralrs121909811
openSNPrs121909811
23andMers121909811
23andMe allrs121909811
SNP Nexus

SNPshotrs121909811
SNPdbers121909811
MSV3drs121909811
GWAS Ctlgrs121909811
StatusMerged into rs33985847
Max Magnitude
OMIM141900
Desc
Variant0127
Relatedalso

[PMID 163659] Hemoglobin J-Chicago (beta76(E20) Ala yields Asp): a new hemoglobin variant resulting from substitution of an external residue.


[PMID 9494051] A case of Hb J-Chicago [beta 76(E20)Ala-->Asp] in a Spanish family.