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rs33958637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33958637(A;G)
Make rs33958637(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5225717
GeneHBB
is asnp
is mentioned by
dbSNPrs33958637
ebirs33958637
HLIrs33958637
Exacrs33958637
Varsomers33958637
Maprs33958637
PheGenIrs33958637
hapmaprs33958637
1000 genomesrs33958637
hgdprs33958637
ensemblrs33958637
gopubmedrs33958637
geneviewrs33958637
scholarrs33958637
googlers33958637
pharmgkbrs33958637
gwascentralrs33958637
openSNPrs33958637
23andMers33958637
23andMe allrs33958637
SNP Nexus

SNPshotrs33958637
SNPdbers33958637
MSV3drs33958637
GWAS Ctlgrs33958637
Max Magnitude0
OMIM141900
Desc
Variant0306
Relatedalso
ClinVar
Risk rs33958637(C,G;C,G)
Alt rs33958637(C,G;C,G)
Reference rs33958637(A;A)
Significance Other
Disease HEMOGLOBIN YOSHIZUKA
Variation info
Gene HBB
CLNDBN HEMOGLOBIN YOSHIZUKA
Reversed 1
HGVS NC_000011.9:g.5246947T>C
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016649.2,


[PMID 5355345OA-icon.png] Hemoglobin Yoshizuka (G10(108)beta asparagine--aspartic acid): a new variant with a reduced oxygen affinity from a Japanese family.