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rs33967561

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33967561(A;G)
Make rs33967561(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position176985
GeneHBA1
is asnp
is mentioned by
dbSNPrs33967561
ebirs33967561
HLIrs33967561
Exacrs33967561
Varsomers33967561
Maprs33967561
PheGenIrs33967561
hapmaprs33967561
1000 genomesrs33967561
hgdprs33967561
ensemblrs33967561
gopubmedrs33967561
geneviewrs33967561
scholarrs33967561
googlers33967561
pharmgkbrs33967561
gwascentralrs33967561
openSNPrs33967561
23andMers33967561
23andMe allrs33967561
SNP Nexus

SNPshotrs33967561
SNPdbers33967561
MSV3drs33967561
GWAS Ctlgrs33967561
Max Magnitude0
OMIM141800
Desc
Variant0001
Relatedalso
ClinVar
Risk rs33967561(G,T;G,T)
Alt rs33967561(G,T;G,T)
Reference rs33967561(A;A)
Significance Other
Disease HEMOGLOBIN AICHI
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN AICHI
Reversed 0
HGVS NC_000016.9:g.226984A>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016986.2,


[PMID 6714429] Hemoglobin Aichi [alpha 50(CE8) His----Arg]: a new slightly unstable hemoglobin variant discovered in Japan.


[PMID 11482884] Rapid identification of hemoglobin variants by electrospray ionization mass spectrometry.