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rs34807671

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs34807671(C;T)
Make rs34807671(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5253282
GeneHBG2, ZNF285B
is asnp
is mentioned by
dbSNPrs34807671
ebirs34807671
HLIrs34807671
Exacrs34807671
Varsomers34807671
Maprs34807671
PheGenIrs34807671
hapmaprs34807671
1000 genomesrs34807671
hgdprs34807671
ensemblrs34807671
gopubmedrs34807671
geneviewrs34807671
scholarrs34807671
googlers34807671
pharmgkbrs34807671
gwascentralrs34807671
openSNPrs34807671
23andMers34807671
23andMe allrs34807671
SNP Nexus

SNPshotrs34807671
SNPdbers34807671
MSV3drs34807671
GWAS Ctlgrs34807671
Max Magnitude0
? (C;C) (C;T) (T;T) 28
OMIM142250
Desc
Variant0032
Relatedalso


ClinVar
Risk rs34807671(T;T)
Alt rs34807671(T;T)
Reference rs34807671(C;C)
Significance Other
Disease HEMOGLOBIN F (ONODA)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (ONODA)
Reversed 1
HGVS NC_000011.9:g.5274512G>A
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016128.1,



[PMID 1703139] Hb F-Onoda or alpha 2G gamma 2(146)(HC3)His----Tyr, a newly discovered fetal hemoglobin variant in a Japanese newborn.