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rs35669628

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs35669628(A;A)
Make rs35669628(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5225635
GeneHBB
is asnp
is mentioned by
dbSNPrs35669628
ebirs35669628
HLIrs35669628
Exacrs35669628
Varsomers35669628
Maprs35669628
PheGenIrs35669628
hapmaprs35669628
1000 genomesrs35669628
hgdprs35669628
ensemblrs35669628
gopubmedrs35669628
geneviewrs35669628
scholarrs35669628
googlers35669628
pharmgkbrs35669628
gwascentralrs35669628
openSNPrs35669628
23andMers35669628
23andMe allrs35669628
SNP Nexus

SNPshotrs35669628
SNPdbers35669628
MSV3drs35669628
GWAS Ctlgrs35669628
Max Magnitude0
OMIM141900
Desc
Variant0442
Relatedalso


ClinVar
Risk rs35669628(A,T;A,T)
Alt rs35669628(A,T;A,T)
Reference rs35669628(C;C)
Significance Other
Disease HEMOGLOBIN BECKMAN
Variation info
Gene HBB
CLNDBN HEMOGLOBIN BECKMAN
Reversed 1
HGVS NC_000011.9:g.5246865G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016796.3,