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rs33976776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs33976776(A;G)
Make rs33976776(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position177096
GeneHBA1
is asnp
is mentioned by
dbSNPrs33976776
ebirs33976776
HLIrs33976776
Exacrs33976776
Varsomers33976776
Maprs33976776
PheGenIrs33976776
hapmaprs33976776
1000 genomesrs33976776
hgdprs33976776
ensemblrs33976776
gopubmedrs33976776
geneviewrs33976776
scholarrs33976776
googlers33976776
pharmgkbrs33976776
gwascentralrs33976776
openSNPrs33976776
23andMers33976776
23andMe allrs33976776
SNP Nexus

SNPshotrs33976776
SNPdbers33976776
MSV3drs33976776
GWAS Ctlgrs33976776
Max Magnitude0
OMIM141800
Desc
Variant0057
Relatedalso
ClinVar
Risk rs33976776(C;C) rs33976776(G;G)
Alt rs33976776(C;C) rs33976776(G;G)
Reference Rs33976776(A;A)
Significance Other
Disease HEMOGLOBIN IWATA
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN IWATA
Reversed 0
HGVS NC_000016.9:g.227095A>G
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000017056.2,


[PMID 6874376] A case of hemoglobin Iwata [alpha 87(F8)His leads to Arg] in China.


[PMID 7419426] Unstable hemoglobins in Japan.