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rs33969953

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs33969953(C;C)
Make rs33969953(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position177063
GeneHBA1
is asnp
is mentioned by
dbSNPrs33969953
ebirs33969953
HLIrs33969953
Exacrs33969953
Varsomers33969953
Maprs33969953
PheGenIrs33969953
hapmaprs33969953
1000 genomesrs33969953
hgdprs33969953
ensemblrs33969953
gopubmedrs33969953
geneviewrs33969953
scholarrs33969953
googlers33969953
pharmgkbrs33969953
gwascentralrs33969953
openSNPrs33969953
23andMers33969953
23andMe allrs33969953
SNP Nexus

SNPshotrs33969953
SNPdbers33969953
MSV3drs33969953
GWAS Ctlgrs33969953
Max Magnitude0
OMIM141800
Desc
Variant0008
Relatedalso
OMIM141800
Desc
Variant0106
Relatedalso
ClinVar
Risk rs33969953(A,C,G;A,C,G)
Alt rs33969953(A,C,G;A,C,G)
Reference rs33969953(T;T)
Significance Other
Disease HEMOGLOBIN NOKO HEMOGLOBIN AZTEC
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN NOKO HEMOGLOBIN AZTEC
Reversed 0
HGVS NC_000016.9:g.227062T>A; NC_000016.9:g.227062T>C
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000017120.2, RCV000016994.2,


[PMID 7275668] Hemoglobinopathies in Japan.


[PMID 3935608] Hb Aztec or alpha 2 76 (EF5) Met----Thr beta 2 detection of a silent mutant by high performance liquid chromatography.


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