Have questions? Visit https://www.reddit.com/r/SNPedia

rs33974277

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
(GG;GG) 0 common in clinvar
Make rs33974277(A;A)
Make rs33974277(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226934
GeneHBB
is asnp
is mentioned by
dbSNPrs33974277
ebirs33974277
HLIrs33974277
Exacrs33974277
Varsomers33974277
Maprs33974277
PheGenIrs33974277
hapmaprs33974277
1000 genomesrs33974277
hgdprs33974277
ensemblrs33974277
gopubmedrs33974277
geneviewrs33974277
scholarrs33974277
googlers33974277
pharmgkbrs33974277
gwascentralrs33974277
openSNPrs33974277
23andMers33974277
23andMe allrs33974277
SNP Nexus

SNPshotrs33974277
SNPdbers33974277
MSV3drs33974277
GWAS Ctlgrs33974277
Merged fromRs121909831
Max Magnitude0
OMIM141900
Desc
Variant0526
Relatedalso
ClinVar
Risk rs33974277(A;A)
Alt rs33974277(A;A)
Reference rs33974277(G;G)
Significance Other
Disease HEMOGLOBIN TIZI-OUZOU
Variation info
Gene HBB
CLNDBN HEMOGLOBIN TIZI-OUZOU
Reversed 1
HGVS NC_000011.9:g.5248164C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016882.2,


[PMID 15481887] Two new beta-chain variants: Hb Tripoli [beta26(B8)Glu-->Ala] and Hb Tizi-Ouzou [beta29(B11)Gly-->Ser].