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rs35286210

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35286210(C;C)
Make rs35286210(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226663
GeneHBB
is asnp
is mentioned by
dbSNPrs35286210
ebirs35286210
HLIrs35286210
Exacrs35286210
Varsomers35286210
Maprs35286210
PheGenIrs35286210
hapmaprs35286210
1000 genomesrs35286210
hgdprs35286210
ensemblrs35286210
gopubmedrs35286210
geneviewrs35286210
scholarrs35286210
googlers35286210
pharmgkbrs35286210
gwascentralrs35286210
openSNPrs35286210
23andMers35286210
23andMe allrs35286210
SNP Nexus

SNPshotrs35286210
SNPdbers35286210
MSV3drs35286210
GWAS Ctlgrs35286210
Max Magnitude0
OMIM141900
Desc
Variant0396
Relatedalso


ClinVar
Risk rs35286210(C;C)
Alt rs35286210(C;C)
Reference rs35286210(G;G)
Significance Other
Disease HEMOGLOBIN CALAIS
Variation info
Gene HBB
CLNDBN HEMOGLOBIN CALAIS
Reversed 1
HGVS NC_000011.9:g.5247893C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016740.2,