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rs28928885

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs28928885(C;G)
Make rs28928885(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position176746
GeneHBA1
is asnp
is mentioned by
dbSNPrs28928885
ebirs28928885
HLIrs28928885
Exacrs28928885
Varsomers28928885
Maprs28928885
PheGenIrs28928885
hapmaprs28928885
1000 genomesrs28928885
hgdprs28928885
ensemblrs28928885
gopubmedrs28928885
geneviewrs28928885
scholarrs28928885
googlers28928885
pharmgkbrs28928885
gwascentralrs28928885
openSNPrs28928885
23andMers28928885
23andMe allrs28928885
SNP Nexus

SNPshotrs28928885
SNPdbers28928885
MSV3drs28928885
GWAS Ctlgrs28928885
Max Magnitude0
OMIM141800
DescHEMOGLOBIN DELFZICHT
Variant0208
Relatedalso
Neighborrs28928888
Distance28
Neighborrs28928880
Distance44
OMIM141850
Desc
Variant0048
Relatedalso


ClinVar
Risk rs28928885(G;G)
Alt rs28928885(G;G)
Reference rs28928885(C;C)
Significance Other
Disease HEMOGLOBIN DELFZICHT
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN DELFZICHT
Reversed 0
HGVS NC_000016.9:g.226745C>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000017227.2,



[PMID 12144062] Hb delfzicht [alpha9(A7)Asn-->Lys (alpha1)]: a new, clinically silent hemoglobin variant observed in a Dutch patient.