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rs34866629

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs34866629(A;G)
Make rs34866629(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226964
GeneHBB
is asnp
is mentioned by
dbSNPrs34866629
ebirs34866629
HLIrs34866629
Exacrs34866629
Varsomers34866629
Maprs34866629
PheGenIrs34866629
hapmaprs34866629
1000 genomesrs34866629
hgdprs34866629
ensemblrs34866629
gopubmedrs34866629
geneviewrs34866629
scholarrs34866629
googlers34866629
pharmgkbrs34866629
gwascentralrs34866629
openSNPrs34866629
23andMers34866629
23andMe allrs34866629
SNP Nexus

SNPshotrs34866629
SNPdbers34866629
MSV3drs34866629
GWAS Ctlgrs34866629
Max Magnitude0
OMIM141900
Desc
Variant0005
Relatedalso


ClinVar
Risk rs34866629(G;G)
Alt rs34866629(G;G)
Reference rs34866629(A;A)
Significance Other
Disease HEMOGLOBIN ALAMO
Variation info
Gene HBB
CLNDBN HEMOGLOBIN ALAMO
Reversed 1
HGVS NC_000011.9:g.5248194T>C
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000016246.2,



[PMID 914645] Hemoglobin Alamo (alpha2beta2 19 (b1) Asn replaced by Asp).