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rs34776279

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34776279(A;A)
Make rs34776279(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position176798
GeneHBA1
is asnp
is mentioned by
dbSNPrs34776279
ebirs34776279
HLIrs34776279
Exacrs34776279
Varsomers34776279
Maprs34776279
PheGenIrs34776279
hapmaprs34776279
1000 genomesrs34776279
hgdprs34776279
ensemblrs34776279
gopubmedrs34776279
geneviewrs34776279
scholarrs34776279
googlers34776279
pharmgkbrs34776279
gwascentralrs34776279
openSNPrs34776279
23andMers34776279
23andMe allrs34776279
SNP Nexus

SNPshotrs34776279
SNPdbers34776279
MSV3drs34776279
GWAS Ctlgrs34776279
Max Magnitude0
OMIM141800
Desc
Variant0134
Relatedalso
ClinVar
Risk rs34776279(A;A)
Alt rs34776279(A;A)
Reference rs34776279(G;G)
Significance Other
Disease HEMOGLOBIN SHUANGFENG
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN SHUANGFENG
Reversed 0
HGVS NC_000016.9:g.226797G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017156.2,


[PMID 3932017] Oxygen equilibrium characteristics of four abnormal hemoglobins found in Hunan.


[PMID 7338471] Hemoglobin Shuangfeng (alpha 27 (B8) Glu substituting for Lys): a new unstable hemoglobin variant.