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rs28928882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs28928882(A;A)
Make rs28928882(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position173248
GeneHBA2
is asnp
is mentioned by
dbSNPrs28928882
ebirs28928882
HLIrs28928882
Exacrs28928882
Varsomers28928882
Maprs28928882
PheGenIrs28928882
hapmaprs28928882
1000 genomesrs28928882
hgdprs28928882
ensemblrs28928882
gopubmedrs28928882
geneviewrs28928882
scholarrs28928882
googlers28928882
pharmgkbrs28928882
gwascentralrs28928882
openSNPrs28928882
23andMers28928882
23andMe allrs28928882
SNP Nexus

SNPshotrs28928882
SNPdbers28928882
MSV3drs28928882
GWAS Ctlgrs28928882
Max Magnitude0
OMIM141800
DescHEMOGLOBIN GOUDA
Variant0198
Relatedalso
Neighborrs28928875
Distance4


ClinVar
Risk rs28928882(A;A)
Alt rs28928882(A;A)
Reference rs28928882(C;C)
Significance Other
Disease HEMOGLOBIN GOUDA
Variation info
Gene HBA2
CLNDBN HEMOGLOBIN GOUDA
Reversed 0
HGVS NC_000016.9:g.223247C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017217.1,



[PMID 8745429] HB Gouda [alpha 72(EF1)His-->Gln], a new silent alpha chain variant.