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rs35662066

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0
Make rs35662066(-;-)
Make rs35662066(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226971
GeneHBB
is asnp
is mentioned by
dbSNPrs35662066
ebirs35662066
HLIrs35662066
Exacrs35662066
Varsomers35662066
Maprs35662066
PheGenIrs35662066
hapmaprs35662066
1000 genomesrs35662066
hgdprs35662066
ensemblrs35662066
gopubmedrs35662066
geneviewrs35662066
scholarrs35662066
googlers35662066
pharmgkbrs35662066
gwascentralrs35662066
openSNPrs35662066
23andMers35662066
23andMe allrs35662066
SNP Nexus

SNPshotrs35662066
SNPdbers35662066
MSV3drs35662066
GWAS Ctlgrs35662066
Max Magnitude0
ClinVar
Risk rs35662066(;)
Alt rs35662066(;)
Reference rs35662066(C;C)
Significance Pathogenic
Disease beta^0^ Thalassemia beta Thalassemia
Variation info
Gene HBB
CLNDBN beta^0^ Thalassemia beta Thalassemia
Reversed 1
HGVS NC_000011.9:g.5248201delG
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016670.26, RCV000173145.1,