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rs34988734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs34988734(C;T)
Make rs34988734(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position177101
GeneHBA1
is asnp
is mentioned by
dbSNPrs34988734
ebirs34988734
HLIrs34988734
Exacrs34988734
Varsomers34988734
Maprs34988734
PheGenIrs34988734
hapmaprs34988734
1000 genomesrs34988734
hgdprs34988734
ensemblrs34988734
gopubmedrs34988734
geneviewrs34988734
scholarrs34988734
googlers34988734
pharmgkbrs34988734
gwascentralrs34988734
openSNPrs34988734
23andMers34988734
23andMe allrs34988734
SNP Nexus

SNPshotrs34988734
SNPdbers34988734
MSV3drs34988734
GWAS Ctlgrs34988734
Max Magnitude0
OMIM141800
Desc
Variant0213
Relatedalso


ClinVar
Risk rs34988734(T;T)
Alt rs34988734(T;T)
Reference rs34988734(C;C)
Significance Other
Disease HEMOGLOBIN VILLEURBANNE
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN VILLEURBANNE
Reversed 0
HGVS NC_000016.9:g.227100C>T
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000017232.2,



[PMID 9269086] Combined mass spectrometric methods for the characterization of human hemoglobin variants localized within alpha T9 peptide: identification of Hb Villeurbanne alpha 89 (FG1) His-->Tyr.