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rs35209776

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs35209776(A;A)
Make rs35209776(A;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5225691
GeneHBB
is asnp
is mentioned by
dbSNPrs35209776
ebirs35209776
HLIrs35209776
Exacrs35209776
Varsomers35209776
Maprs35209776
PheGenIrs35209776
hapmaprs35209776
1000 genomesrs35209776
hgdprs35209776
ensemblrs35209776
gopubmedrs35209776
geneviewrs35209776
scholarrs35209776
googlers35209776
pharmgkbrs35209776
gwascentralrs35209776
openSNPrs35209776
23andMers35209776
23andMe allrs35209776
SNP Nexus

SNPshotrs35209776
SNPdbers35209776
MSV3drs35209776
GWAS Ctlgrs35209776
Max Magnitude0
OMIM141900
Desc
Variant0097
Relatedalso
ClinVar
Risk rs35209776(A,G;A,G)
Alt rs35209776(A,G;A,G)
Reference rs35209776(T;T)
Significance Other
Disease HEMOGLOBIN HAFNIA
Variation info
Gene HBB
CLNDBN HEMOGLOBIN HAFNIA
Reversed 1
HGVS NC_000011.10:g.5225691A>Y
CLNSRC OMIM Allelic Variant
CLNACC RCV000016368.1,


[PMID 3395624] Hemoglobin hafnia: alpha 2 (beta 116 (G18) His----Gln)2; a new hemoglobin variant mistaken for glycated hemoglobin.