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rs33919924

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33919924(A;C)
Make rs33919924(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226734
GeneHBB
is asnp
is mentioned by
dbSNPrs33919924
ebirs33919924
HLIrs33919924
Exacrs33919924
Varsomers33919924
Maprs33919924
PheGenIrs33919924
hapmaprs33919924
1000 genomesrs33919924
hgdprs33919924
ensemblrs33919924
gopubmedrs33919924
geneviewrs33919924
scholarrs33919924
googlers33919924
pharmgkbrs33919924
gwascentralrs33919924
openSNPrs33919924
23andMers33919924
23andMe allrs33919924
SNP Nexus

SNPshotrs33919924
SNPdbers33919924
MSV3drs33919924
GWAS Ctlgrs33919924
Max Magnitude0
OMIM141900
Desc
Variant0203
Relatedalso
OMIM141900
Desc
Variant0531
Relatedalso
ClinVar
Risk rs33919924(C,G,T;C,G,T)
Alt rs33919924(C,G,T;C,G,T)
Reference rs33919924(A;A)
Significance Other
Disease HEMOGLOBIN HOKUSETSU HEMOGLOBIN OCHO RIOS
Variation info
Gene HBB
CLNDBN HEMOGLOBIN HOKUSETSU HEMOGLOBIN OCHO RIOS
Reversed 1
HGVS NC_000011.9:g.5247964T>C; NC_000011.9:g.5247964T>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016825.2, RCV000016526.2,


[PMID 5046622OA-icon.png] Haemoglobin Ocho Rios ( beta52 (D3) aspartic acid leads to alanine): a new beta-chain variant of haemoglobin A found in combination with haemoglobin S.


[PMID 9730366] A new hemoglobin variant found during Hb A1c measurement: Hb Hokusetsu [beta52(D3)Asp-->Gly].