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rs34173382

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs34173382(A;G)
Make rs34173382(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226653
GeneHBB
is asnp
is mentioned by
dbSNPrs34173382
ebirs34173382
HLIrs34173382
Exacrs34173382
Varsomers34173382
Maprs34173382
PheGenIrs34173382
hapmaprs34173382
1000 genomesrs34173382
hgdprs34173382
ensemblrs34173382
gopubmedrs34173382
geneviewrs34173382
scholarrs34173382
googlers34173382
pharmgkbrs34173382
gwascentralrs34173382
openSNPrs34173382
23andMers34173382
23andMe allrs34173382
SNP Nexus

SNPshotrs34173382
SNPdbers34173382
MSV3drs34173382
GWAS Ctlgrs34173382
Max Magnitude0
OMIM141900
Desc
Variant0084
Relatedalso


ClinVar
Risk rs34173382(G;G)
Alt rs34173382(G;G)
Reference rs34173382(A;A)
Significance Other
Disease HEMOGLOBIN G (HSI-TSOU)
Variation info
Gene HBB
CLNDBN HEMOGLOBIN G (HSI-TSOU)
Reversed 1
HGVS NC_000011.9:g.5247883T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016351.2,



[PMID 5009835] Hemoglobin G Hsi-Tsou: 79 Asp to Gly.