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rs33956555

From SNPedia

Orientationminus
Stabilizedminus
Make rs33956555(C;C)
Make rs33956555(C;G)
Make rs33956555(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226798
GeneHBB
is asnp
is mentioned by
dbSNPrs33956555
ebirs33956555
HLIrs33956555
Exacrs33956555
Varsomers33956555
Maprs33956555
PheGenIrs33956555
hapmaprs33956555
1000 genomesrs33956555
hgdprs33956555
ensemblrs33956555
gopubmedrs33956555
geneviewrs33956555
scholarrs33956555
googlers33956555
pharmgkbrs33956555
gwascentralrs33956555
openSNPrs33956555
23andMers33956555
23andMe allrs33956555
SNP Nexus

SNPshotrs33956555
SNPdbers33956555
MSV3drs33956555
GWAS Ctlgrs33956555
Merged fromRs111033584
Max Magnitude

[PMID 11976817] Characterization of a new hemoglobin variant: Hb Badalona (beta31[B13]Leu-->Val).

ClinVar
Risk rs33956555(G,T;G,T)
Alt rs33956555(G,T;G,T)
Reference rs33956555(C;C)
Significance Other
Disease HEMOGLOBIN MUSCAT
Variation info
Gene HBB
CLNDBN HEMOGLOBIN MUSCAT
Reversed 1
HGVS NC_000011.9:g.5248028G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016771.2,