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rs34743882

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34743882(A;A)
Make rs34743882(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226753
GeneHBB
is asnp
is mentioned by
dbSNPrs34743882
ebirs34743882
HLIrs34743882
Exacrs34743882
Varsomers34743882
Maprs34743882
PheGenIrs34743882
hapmaprs34743882
1000 genomesrs34743882
hgdprs34743882
ensemblrs34743882
gopubmedrs34743882
geneviewrs34743882
scholarrs34743882
googlers34743882
pharmgkbrs34743882
gwascentralrs34743882
openSNPrs34743882
23andMers34743882
23andMe allrs34743882
SNP Nexus

SNPshotrs34743882
SNPdbers34743882
MSV3drs34743882
GWAS Ctlgrs34743882
Max Magnitude0
OMIM141900
Desc
Variant0090
Relatedalso
ClinVar
Risk rs34743882(A;A)
Alt rs34743882(A;A)
Reference rs34743882(G;G)
Significance Other
Disease HEMOGLOBIN GAINESVILLE-GA
Variation info
Gene HBB
CLNDBN HEMOGLOBIN GAINESVILLE-GA
Reversed 1
HGVS NC_000011.9:g.5247983C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016358.2,


[PMID 2481659] Hb Gainesville-GA or alpha 2 beta 2(46)(CD5)Gly----Arg; second report.


[PMID 3839773] Hb Gainesville-GA or alpha 2 beta 2 46(CD5)Gly----Arg.