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rs281864894

From SNPedia

Orientationminus
Stabilizedminus
Make rs281864894(C;C)
Make rs281864894(C;T)
Make rs281864894(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226738
GeneHBB
is asnp
is mentioned by
dbSNPrs281864894
dbSNP (old)rs281864894
ClinGenrs281864894
ebirs281864894
HLIrs281864894
Exacrs281864894
Gnomadrs281864894
Varsomers281864894
Maprs281864894
PheGenIrs281864894
Biobankrs281864894
1000 genomesrs281864894
hgdprs281864894
ensemblrs281864894
gopubmedrs281864894
geneviewrs281864894
scholarrs281864894
googlers281864894
pharmgkbrs281864894
gwascentralrs281864894
openSNPrs281864894
23andMers281864894
23andMe allrs281864894
SNP Nexus

SNPshotrs281864894
SNPdbers281864894
MSV3drs281864894
GWAS Ctlgrs281864894
Merged fromRs33930476
Max Magnitude

[PMID 2079433] New results of hemoglobin variant structure determinations by fast atom bombardment mass spectrometry.

ClinVar
Risk rs281864894(T;T)
Alt rs281864894(T;T)
Reference rs281864894(C;C)
Significance Other
Disease HEMOGLOBIN GRENOBLE
Variation info
Gene HBB
CLNDBN HEMOGLOBIN GRENOBLE
Reversed 1
HGVS NC_000011.9:g.5247968G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016759.2,