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rs34390965

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34390965(G;T)
Make rs34390965(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position5233991
GeneHBD
is asnp
is mentioned by
dbSNPrs34390965
ebirs34390965
HLIrs34390965
Exacrs34390965
Varsomers34390965
Maprs34390965
PheGenIrs34390965
hapmaprs34390965
1000 genomesrs34390965
hgdprs34390965
ensemblrs34390965
gopubmedrs34390965
geneviewrs34390965
scholarrs34390965
googlers34390965
pharmgkbrs34390965
gwascentralrs34390965
openSNPrs34390965
23andMers34390965
23andMe allrs34390965
SNP Nexus

SNPshotrs34390965
SNPdbers34390965
MSV3drs34390965
GWAS Ctlgrs34390965
Max Magnitude0
? (G;G) (G;T) (T;T) 28
OMIM142000
Desc
Variant0042
Relatedalso


ClinVar
Risk rs34390965(T;T)
Alt rs34390965(T;T)
Reference rs34390965(G;G)
Significance Other
Disease HEMOGLOBIN A(2) CAPRI
Variation info
Gene HBD
CLNDBN HEMOGLOBIN A(2) CAPRI
Reversed 1
HGVS NC_000011.9:g.5255221C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016236.1,



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