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rs34629158

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34629158(A;A)
Make rs34629158(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position177313
GeneHBA1
is asnp
is mentioned by
dbSNPrs34629158
ebirs34629158
HLIrs34629158
Exacrs34629158
Varsomers34629158
Maprs34629158
PheGenIrs34629158
hapmaprs34629158
1000 genomesrs34629158
hgdprs34629158
ensemblrs34629158
gopubmedrs34629158
geneviewrs34629158
scholarrs34629158
googlers34629158
pharmgkbrs34629158
gwascentralrs34629158
openSNPrs34629158
23andMers34629158
23andMe allrs34629158
SNP Nexus

SNPshotrs34629158
SNPdbers34629158
MSV3drs34629158
GWAS Ctlgrs34629158
Merged fromRs63750629
Max Magnitude0
OMIM141800
Desc
Variant0162
Relatedalso


ClinVar
Risk rs34629158(A;A)
Alt rs34629158(A;A)
Reference rs34629158(G;G)
Significance Other
Disease HEMOGLOBIN TONOSHO
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN TONOSHO
Reversed 0
HGVS NC_000016.9:g.227312G>A
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000017183.2,



[PMID 2283295] A new alpha chain variant Hb Tonosho [alpha 110(G17)Ala----Thr]: subunit dissociation during cation exchange chromatography for Hb A1c assay.