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rs34571024

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs34571024(A;C)
Make rs34571024(C;C)
ReferenceGRCh38 38.1/142
Chromosome11
Position5226777
GeneHBB
is asnp
is mentioned by
dbSNPrs34571024
ebirs34571024
HLIrs34571024
Exacrs34571024
Varsomers34571024
Maprs34571024
PheGenIrs34571024
hapmaprs34571024
1000 genomesrs34571024
hgdprs34571024
ensemblrs34571024
gopubmedrs34571024
geneviewrs34571024
scholarrs34571024
googlers34571024
pharmgkbrs34571024
gwascentralrs34571024
openSNPrs34571024
23andMers34571024
23andMe allrs34571024
SNP Nexus

SNPshotrs34571024
SNPdbers34571024
MSV3drs34571024
GWAS Ctlgrs34571024
Max Magnitude0
OMIM141900
Desc
Variant0101
Relatedalso


ClinVar
Risk rs34571024(C;C)
Alt rs34571024(C;C)
Reference rs34571024(A;A)
Significance Other
Disease HEMOGLOBIN HAZEBROUCK
Variation info
Gene HBB
CLNDBN HEMOGLOBIN HAZEBROUCK
Reversed 1
HGVS NC_000011.9:g.5248007T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016374.2,



[PMID 6430717] Structural study of hemoglobin Hazebrouck, beta 38(C4)Thr----Pro. A new abnormal hemoglobin with instability and low oxygen affinity.