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rs34933313

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs34933313(C;G)
Make rs34933313(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5234041
GeneHBD
is asnp
is mentioned by
dbSNPrs34933313
ebirs34933313
HLIrs34933313
Exacrs34933313
Varsomers34933313
Maprs34933313
PheGenIrs34933313
hapmaprs34933313
1000 genomesrs34933313
hgdprs34933313
ensemblrs34933313
gopubmedrs34933313
geneviewrs34933313
scholarrs34933313
googlers34933313
pharmgkbrs34933313
gwascentralrs34933313
openSNPrs34933313
23andMers34933313
23andMe allrs34933313
SNP Nexus

SNPshotrs34933313
SNPdbers34933313
MSV3drs34933313
GWAS Ctlgrs34933313
Max Magnitude0
OMIM142000
Desc
Variant0041
Relatedalso


ClinVar
Risk rs34933313(G;G)
Alt rs34933313(G;G)
Reference rs34933313(C;C)
Significance Other
Disease HEMOGLOBIN A(2) LUCANIA
Variation info
Gene HBD
CLNDBN HEMOGLOBIN A(2) LUCANIA
Reversed 1
HGVS NC_000011.9:g.5255271G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016235.1,



[PMID 12402333] Epidemiology of the delta globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features.