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rs35834416

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs35834416(G;G)
Make rs35834416(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5225651
GeneHBB
is asnp
is mentioned by
dbSNPrs35834416
ebirs35834416
HLIrs35834416
Exacrs35834416
Varsomers35834416
Maprs35834416
PheGenIrs35834416
hapmaprs35834416
1000 genomesrs35834416
hgdprs35834416
ensemblrs35834416
gopubmedrs35834416
geneviewrs35834416
scholarrs35834416
googlers35834416
pharmgkbrs35834416
gwascentralrs35834416
openSNPrs35834416
23andMers35834416
23andMe allrs35834416
SNP Nexus

SNPshotrs35834416
SNPdbers35834416
MSV3drs35834416
GWAS Ctlgrs35834416
Max Magnitude0
OMIM141900
Desc
Variant0297
Relatedalso


ClinVar
Risk rs35834416(G;G)
Alt rs35834416(G;G)
Reference rs35834416(T;T)
Significance Other
Disease HEMOGLOBIN WIEN
Variation info
Gene HBB
CLNDBN HEMOGLOBIN WIEN
Reversed 1
HGVS NC_000011.9:g.5246881A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016641.2,



[PMID 4212355] Structure of haemoglobin Wien beta 130 (H8) tyrosine-aspartic acid: an unstable haemoglobin variant.


[PMID 5081733] [Properties of the unstable Hb Wien].