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rs34098449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs34098449(A;A)
Make rs34098449(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position177291
GeneHBA1
is asnp
is mentioned by
dbSNPrs34098449
ebirs34098449
HLIrs34098449
Exacrs34098449
Varsomers34098449
Maprs34098449
PheGenIrs34098449
hapmaprs34098449
1000 genomesrs34098449
hgdprs34098449
ensemblrs34098449
gopubmedrs34098449
geneviewrs34098449
scholarrs34098449
googlers34098449
pharmgkbrs34098449
gwascentralrs34098449
openSNPrs34098449
23andMers34098449
23andMe allrs34098449
SNP Nexus

SNPshotrs34098449
SNPdbers34098449
MSV3drs34098449
GWAS Ctlgrs34098449
Max Magnitude0
OMIM141850
Desc
Variant0047
Relatedalso


ClinVar
Risk rs34098449(A;A)
Alt rs34098449(A;A)
Reference rs34098449(C;C)
Significance Untested
Disease
Variation info
Gene HBA1
CLNDBN
Reversed 0
HGVS NC_000016.9:g.227290C>A
CLNSRC
CLNACC



[PMID 87] Some physicochemical properties of hemoglobin-manitoba (alpha2 102Ser replaced by Arg (G9) beta2).


[PMID 5452728] alpha 102(G9) serine replaced by arginine.


[PMID 6547932] The characterization of hemoglobin Manitoba or alpha (2)102(G9)Ser----Arg beta 2 and hemoglobin Contaldo or alpha (2)103(G10)His----Arg beta 2 by high performance liquid chromatography.


[PMID 7803274] The differences in quantities of alpha 2- and alpha 1-globin gene variants in heterozygotes.