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rs33988732

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33988732(A;G)
Make rs33988732(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226720
GeneHBB
is asnp
is mentioned by
dbSNPrs33988732
ebirs33988732
HLIrs33988732
Exacrs33988732
Varsomers33988732
Maprs33988732
PheGenIrs33988732
hapmaprs33988732
1000 genomesrs33988732
hgdprs33988732
ensemblrs33988732
gopubmedrs33988732
geneviewrs33988732
scholarrs33988732
googlers33988732
pharmgkbrs33988732
gwascentralrs33988732
openSNPrs33988732
23andMers33988732
23andMe allrs33988732
SNP Nexus

SNPshotrs33988732
SNPdbers33988732
MSV3drs33988732
GWAS Ctlgrs33988732
Max Magnitude0
OMIM141900
Desc
Variant0129
Relatedalso
ClinVar
Risk rs33988732(C,G;C,G)
Alt rs33988732(C,G;C,G)
Reference rs33988732(A;A)
Significance Other
Disease HEMOGLOBIN J (DALOA)
Variation info
Gene HBB
CLNDBN HEMOGLOBIN J (DALOA)
Reversed 1
HGVS NC_000011.9:g.5247950T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016415.2,


[PMID 6292136] Hb J Daloa (beta 57 (E1) Asn replaced by Asp): a new variant found in Ivory Coast.