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rs35278874

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs35278874(C;G)
Make rs35278874(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226718
GeneHBB
is asnp
is mentioned by
dbSNPrs35278874
ebirs35278874
HLIrs35278874
Exacrs35278874
Varsomers35278874
Maprs35278874
PheGenIrs35278874
hapmaprs35278874
1000 genomesrs35278874
hgdprs35278874
ensemblrs35278874
gopubmedrs35278874
geneviewrs35278874
scholarrs35278874
googlers35278874
pharmgkbrs35278874
gwascentralrs35278874
openSNPrs35278874
23andMers35278874
23andMe allrs35278874
SNP Nexus

SNPshotrs35278874
SNPdbers35278874
MSV3drs35278874
GWAS Ctlgrs35278874
Max Magnitude0
OMIM141900
Desc
Variant0082
Relatedalso
ClinVar
Risk rs35278874(A,G,T;A,G,T)
Alt rs35278874(A,G,T;A,G,T)
Reference rs35278874(C;C)
Significance Other
Disease HEMOGLOBIN G (FERRARA)
Variation info
Gene HBB
CLNDBN HEMOGLOBIN G (FERRARA)
Reversed 1
HGVS NC_000011.9:g.5247948G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016347.2,


[PMID 26414] Properties of hemoglobin G. Ferrara (beta57(E1) Asn replaced by Lys).