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rs34830032

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs34830032(C;G)
Make rs34830032(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position177319
GeneHBA1
is asnp
is mentioned by
dbSNPrs34830032
ebirs34830032
HLIrs34830032
Exacrs34830032
Varsomers34830032
Maprs34830032
PheGenIrs34830032
hapmaprs34830032
1000 genomesrs34830032
hgdprs34830032
ensemblrs34830032
gopubmedrs34830032
geneviewrs34830032
scholarrs34830032
googlers34830032
pharmgkbrs34830032
gwascentralrs34830032
openSNPrs34830032
23andMers34830032
23andMe allrs34830032
SNP Nexus

SNPshotrs34830032
SNPdbers34830032
MSV3drs34830032
GWAS Ctlgrs34830032
Merged fromRs63749881
Max Magnitude0
OMIM141800
Desc
Variant0054
Relatedalso
ClinVar
Risk rs34830032(G;G)
Alt rs34830032(G;G)
Reference rs34830032(C;C)
Significance Other
Disease HEMOGLOBIN HOPKINS 2
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN HOPKINS 2
Reversed 0
HGVS NC_000016.9:g.227318C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017050.3,


[PMID 646867] The structure of hemoglobin Hopkins-2.


[PMID 5288820] Clinical studies and physiological properties of Hopkins-2 haemoglobin.