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rs34263826

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs34263826(A;G)
Make rs34263826(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5254712
GeneHBG2
is asnp
is mentioned by
dbSNPrs34263826
ebirs34263826
HLIrs34263826
Exacrs34263826
Varsomers34263826
Maprs34263826
PheGenIrs34263826
hapmaprs34263826
1000 genomesrs34263826
hgdprs34263826
ensemblrs34263826
gopubmedrs34263826
geneviewrs34263826
scholarrs34263826
googlers34263826
pharmgkbrs34263826
gwascentralrs34263826
openSNPrs34263826
23andMers34263826
23andMe allrs34263826
SNP Nexus

SNPshotrs34263826
SNPdbers34263826
MSV3drs34263826
GWAS Ctlgrs34263826
Max Magnitude0
OMIM142200
Desc
Variant0014
Relatedalso
OMIM142250
Desc
Variant0016
Relatedalso


ClinVar
Risk rs34263826(G;G)
Alt rs34263826(G;G)
Reference rs34263826(A;A)
Significance Other
Disease HEMOGLOBIN F (MEINOHAMA)
Variation info
Gene HBG2
CLNDBN HEMOGLOBIN F (MEINOHAMA)
Reversed 1
HGVS NC_000011.9:g.5275942T>C
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016112.1,



[PMID 6172403] Hb F-Meinohama or alpha 2 gamma 2 (5 Glu replaced by Gly; 75 Ile; 136 Gly).