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rs33930476

From SNPedia

Merged intors281864894
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(CC;CC) 0 common in clinvar
Make rs33930476(C;T)
Make rs33930476(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226738
GeneHBB
is asnp
is mentioned by
dbSNPrs33930476
ebirs33930476
HLIrs33930476
Exacrs33930476
Varsomers33930476
Maprs33930476
PheGenIrs33930476
hapmaprs33930476
1000 genomesrs33930476
hgdprs33930476
ensemblrs33930476
gopubmedrs33930476
geneviewrs33930476
scholarrs33930476
googlers33930476
pharmgkbrs33930476
gwascentralrs33930476
openSNPrs33930476
23andMers33930476
23andMe allrs33930476
SNP Nexus

SNPshotrs33930476
SNPdbers33930476
MSV3drs33930476
GWAS Ctlgrs33930476
StatusMerged into rs281864894
Max Magnitude0
OMIM141900
Desc
Variant0408
Relatedalso
ClinVar
Risk rs33930476(TC,C;TC,C)
Alt rs33930476(TC,C;TC,C)
Reference rs33930476(CC;CC)
Significance Untested
Disease
Variation info
Gene HBB
CLNDBN
Reversed 1
HGVS NC_000011.9:g.5247968G>A
CLNSRC
CLNACC