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rs34404985

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34404985(C;C)
Make rs34404985(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226946
GeneHBB
is asnp
is mentioned by
dbSNPrs34404985
ebirs34404985
HLIrs34404985
Exacrs34404985
Varsomers34404985
Maprs34404985
PheGenIrs34404985
hapmaprs34404985
1000 genomesrs34404985
hgdprs34404985
ensemblrs34404985
gopubmedrs34404985
geneviewrs34404985
scholarrs34404985
googlers34404985
pharmgkbrs34404985
gwascentralrs34404985
openSNPrs34404985
23andMers34404985
23andMe allrs34404985
SNP Nexus

SNPshotrs34404985
SNPdbers34404985
MSV3drs34404985
GWAS Ctlgrs34404985
Max Magnitude0
OMIM141900
Desc
Variant0089
Relatedalso


ClinVar
Risk rs34404985(A,C;A,C)
Alt rs34404985(A,C;A,C)
Reference rs34404985(G;G)
Significance Other
Disease HEMOGLOBIN G (TAIWAN-AMI)
Variation info
Gene HBB
CLNDBN HEMOGLOBIN G (TAIWAN-AMI)
Reversed 1
HGVS NC_000011.9:g.5248176C>G
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016357.3,



[PMID 5642385] Hemoglobin G Taiwan-Ami: alpha-2-beta-225 Gly--Arg.