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rs33922873

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs33922873(C;T)
Make rs33922873(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226702
GeneHBB
is asnp
is mentioned by
dbSNPrs33922873
ebirs33922873
HLIrs33922873
Exacrs33922873
Varsomers33922873
Maprs33922873
PheGenIrs33922873
hapmaprs33922873
1000 genomesrs33922873
hgdprs33922873
ensemblrs33922873
gopubmedrs33922873
geneviewrs33922873
scholarrs33922873
googlers33922873
pharmgkbrs33922873
gwascentralrs33922873
openSNPrs33922873
23andMers33922873
23andMe allrs33922873
SNP Nexus

SNPshotrs33922873
SNPdbers33922873
MSV3drs33922873
GWAS Ctlgrs33922873
Max Magnitude0
OMIM141900
Desc
Variant0165
Relatedalso
ClinVar
Risk rs33922873(A,T;A,T)
Alt rs33922873(A,T;A,T)
Reference rs33922873(C;C)
Significance Other
Disease HEMOGLOBIN M (SASKATOON)
Variation info
Gene HBB
CLNDBN HEMOGLOBIN M (SASKATOON)
Reversed 1
HGVS NC_000011.9:g.5247932G>A
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016466.4,


[PMID 9601847] [Hemoglobin Hana or alpha 2 beta 2 63 (E7) His-Asn: a new unstable hemoglobin variant with a paradoxically different clinical manifestations in smokers and non-smokers in the same family].