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rs34997902

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs34997902(A;C)
Make rs34997902(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5253344
GeneHBG2
is asnp
is mentioned by
dbSNPrs34997902
ebirs34997902
HLIrs34997902
Exacrs34997902
Varsomers34997902
Maprs34997902
PheGenIrs34997902
hapmaprs34997902
1000 genomesrs34997902
hgdprs34997902
ensemblrs34997902
gopubmedrs34997902
geneviewrs34997902
scholarrs34997902
googlers34997902
pharmgkbrs34997902
gwascentralrs34997902
openSNPrs34997902
23andMers34997902
23andMe allrs34997902
SNP Nexus

SNPshotrs34997902
SNPdbers34997902
MSV3drs34997902
GWAS Ctlgrs34997902
Max Magnitude0
OMIM142250
Desc
Variant0021
Relatedalso


ClinVar
Risk rs34997902(C,T;C,T)
Alt rs34997902(C,T;C,T)
Reference rs34997902(A;A)
Significance Other
Disease HEMOGLOBIN F (PORT ROYAL)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (PORT ROYAL)
Reversed 1
HGVS NC_000011.9:g.5274574T>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016117.1,



[PMID 4846278] Haemoglobin F Port Royal (alpha2G gamma2 125 Glu leads to Ala).