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rs33929459

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs33929459(A;A)
Make rs33929459(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226952
GeneHBB
is asnp
is mentioned by
dbSNPrs33929459
ebirs33929459
HLIrs33929459
Exacrs33929459
Varsomers33929459
Maprs33929459
PheGenIrs33929459
hapmaprs33929459
1000 genomesrs33929459
hgdprs33929459
ensemblrs33929459
gopubmedrs33929459
geneviewrs33929459
scholarrs33929459
googlers33929459
pharmgkbrs33929459
gwascentralrs33929459
openSNPrs33929459
23andMers33929459
23andMe allrs33929459
SNP Nexus

SNPshotrs33929459
SNPdbers33929459
MSV3drs33929459
GWAS Ctlgrs33929459
Max Magnitude0
OMIM141900
Desc
Variant0216
Relatedalso
ClinVar
Risk rs33929459(A,T;A,T)
Alt rs33929459(A,T;A,T)
Reference rs33929459(G;G)
Significance Other
Disease HEMOGLOBIN PALMERSTON NORTH HEMOGLOBIN S (ANTILLES)
Variation info
Gene HBB
CLNDBN HEMOGLOBIN PALMERSTON NORTH HEMOGLOBIN S (ANTILLES)
Reversed 1
HGVS NC_000011.9:g.5248182C>A; NC_000011.9:g.5248182C>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016544.2, RCV000016576.5,


[PMID 7161106] Hemoglobin Palmerston North beta 23 (B5) Val replaced by Phe. A new variant identified in a patient with polycythemia.