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rs34876238

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34876238(A;A)
Make rs34876238(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5254303
GeneHBG2, LOC100288908
is asnp
is mentioned by
dbSNPrs34876238
ebirs34876238
HLIrs34876238
Exacrs34876238
Varsomers34876238
Maprs34876238
PheGenIrs34876238
hapmaprs34876238
1000 genomesrs34876238
hgdprs34876238
ensemblrs34876238
gopubmedrs34876238
geneviewrs34876238
scholarrs34876238
googlers34876238
pharmgkbrs34876238
gwascentralrs34876238
openSNPrs34876238
23andMers34876238
23andMe allrs34876238
SNP Nexus

SNPshotrs34876238
SNPdbers34876238
MSV3drs34876238
GWAS Ctlgrs34876238
Max Magnitude0
OMIM142250
Desc
Variant0011
Relatedalso


ClinVar
Risk rs34876238(A,C;A,C)
Alt rs34876238(A,C;A,C)
Reference rs34876238(G;G)
Significance Other
Disease HEMOGLOBIN F (LA GRANGE)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (LA GRANGE)
Reversed 1
HGVS NC_000011.9:g.5275533C>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016107.1,



[PMID 6206897] Hb F-La Grange or alpha 2 gamma 2 101(G3)Glu----Lys; 75Ile; 136Gly: a high oxygen affinity fetal hemoglobin variant observed in a Caucasian newborn.