Have questions? Visit https://www.reddit.com/r/SNPedia

rs34856846

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs34856846(-;-)
Make rs34856846(-;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226986
GeneHBB
is asnp
is mentioned by
dbSNPrs34856846
ebirs34856846
HLIrs34856846
Exacrs34856846
Varsomers34856846
Maprs34856846
PheGenIrs34856846
hapmaprs34856846
1000 genomesrs34856846
hgdprs34856846
ensemblrs34856846
gopubmedrs34856846
geneviewrs34856846
scholarrs34856846
googlers34856846
pharmgkbrs34856846
gwascentralrs34856846
openSNPrs34856846
23andMers34856846
23andMe allrs34856846
SNP Nexus

SNPshotrs34856846
SNPdbers34856846
MSV3drs34856846
GWAS Ctlgrs34856846
Max Magnitude0
ClinVar
Risk rs34856846(;)
Alt rs34856846(;)
Reference rs34856846(T;T)
Significance Pathogenic
Disease beta^0^ Thalassemia
Variation info
Gene HBB
CLNDBN beta^0^ Thalassemia
Reversed 1
HGVS NC_000011.9:g.5248216delA
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016679.25,



[PMID 1769663] Molecular heterogeneity of beta-thalassemia in mestizo Mexicans.


[PMID 8619407] Haplotype analysis of the Mexican frameshift Cd 11 (-T) and -28 A->C beta-thalassemia alleles.