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rs34071856

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs34071856(G;G)
Make rs34071856(G;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position177075
GeneHBA1
is asnp
is mentioned by
dbSNPrs34071856
ebirs34071856
HLIrs34071856
Exacrs34071856
Varsomers34071856
Maprs34071856
PheGenIrs34071856
hapmaprs34071856
1000 genomesrs34071856
hgdprs34071856
ensemblrs34071856
gopubmedrs34071856
geneviewrs34071856
scholarrs34071856
googlers34071856
pharmgkbrs34071856
gwascentralrs34071856
openSNPrs34071856
23andMers34071856
23andMe allrs34071856
SNP Nexus

SNPshotrs34071856
SNPdbers34071856
MSV3drs34071856
GWAS Ctlgrs34071856
Max Magnitude0
OMIM141800
Desc
Variant0004
Relatedalso
ClinVar
Risk rs34071856(G;G)
Alt rs34071856(G;G)
Reference rs34071856(T;T)
Significance Other
Disease HEMOGLOBIN ANN ARBOR
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN ANN ARBOR
Reversed 0
HGVS NC_000016.9:g.227074T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016990.2,


[PMID 5033650] Biosynthesis of hemoglobin Ann Arbor: evidence for catabolic and feedback regulation.