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rs36107977

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(I;I) 0
Make rs36107977(-;-)
Make rs36107977(-;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226699
GeneHBB
is asnp
is mentioned by
dbSNPrs36107977
ebirs36107977
HLIrs36107977
Exacrs36107977
Varsomers36107977
Maprs36107977
PheGenIrs36107977
hapmaprs36107977
1000 genomesrs36107977
hgdprs36107977
ensemblrs36107977
gopubmedrs36107977
geneviewrs36107977
scholarrs36107977
googlers36107977
pharmgkbrs36107977
gwascentralrs36107977
openSNPrs36107977
23andMers36107977
23andMe allrs36107977
SNP Nexus

SNPshotrs36107977
SNPdbers36107977
MSV3drs36107977
GWAS Ctlgrs36107977
Max Magnitude0
ClinVar
Risk rs36107977(;)
Alt rs36107977(;)
Reference rs36107977(G;G)
Significance Pathogenic
Disease beta^0^ Thalassemia
Variation info
Gene HBB
CLNDBN beta^0^ Thalassemia
Reversed 1
HGVS NC_000011.9:g.5247929delC
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016686.23,



[PMID 2665856] Characterization of a spontaneous mutation in beta-thalassemia associated with advanced paternal age.


[PMID 4512457] New mutation leading to -thalassaemia minor.