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rs33937535

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33937535(A;C)
Make rs33937535(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position5225650
GeneHBB
is asnp
is mentioned by
dbSNPrs33937535
ebirs33937535
HLIrs33937535
Exacrs33937535
Varsomers33937535
Maprs33937535
PheGenIrs33937535
hapmaprs33937535
1000 genomesrs33937535
hgdprs33937535
ensemblrs33937535
gopubmedrs33937535
geneviewrs33937535
scholarrs33937535
googlers33937535
pharmgkbrs33937535
gwascentralrs33937535
openSNPrs33937535
23andMers33937535
23andMe allrs33937535
SNP Nexus

SNPshotrs33937535
SNPdbers33937535
MSV3drs33937535
GWAS Ctlgrs33937535
Max Magnitude0
OMIM141900
Desc
Variant0194
Relatedalso
ClinVar
Risk rs33937535(C,G;C,G)
Alt rs33937535(C,G;C,G)
Reference rs33937535(A;A)
Significance Other
Disease HEMOGLOBIN NEVERS
Variation info
Gene HBB
CLNDBN HEMOGLOBIN NEVERS
Reversed 1
HGVS NC_000011.9:g.5246880T>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016514.2,


[PMID 2384309] Hemoglobin Nevers [alpha 2 beta 2130(H8)Tyr----Ser]; a new silent variant found in France.