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rs34264694

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs34264694(A;C)
Make rs34264694(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5254408
GeneHBG2
is asnp
is mentioned by
dbSNPrs34264694
ClinGenrs34264694
ebirs34264694
HLIrs34264694
Exacrs34264694
Varsomers34264694
Maprs34264694
PheGenIrs34264694
hapmaprs34264694
1000 genomesrs34264694
hgdprs34264694
ensemblrs34264694
gopubmedrs34264694
geneviewrs34264694
scholarrs34264694
googlers34264694
pharmgkbrs34264694
gwascentralrs34264694
openSNPrs34264694
23andMers34264694
23andMe allrs34264694
SNP Nexus

SNPshotrs34264694
SNPdbers34264694
MSV3drs34264694
GWAS Ctlgrs34264694
Max Magnitude0
OMIM142250
Desc
Variant0031
Relatedalso
ClinVar
Risk rs34264694(C;C)
Alt rs34264694(C;C)
Reference Rs34264694(A;A)
Significance Other
Disease HEMOGLOBIN F (BROOKLYN)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (BROOKLYN)
Reversed 1
HGVS NC_000011.9:g.5275638T>G
CLNSRC HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000016127.1,


[PMID 1703138] Hb F-Brooklyn or alpha 2G gamma 2(66)(E10)Lys----Gln.