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rs36038739

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs36038739(G;T)
Make rs36038739(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position5226604
GeneHBB
is asnp
is mentioned by
dbSNPrs36038739
ebirs36038739
HLIrs36038739
Exacrs36038739
Varsomers36038739
Maprs36038739
PheGenIrs36038739
hapmaprs36038739
1000 genomesrs36038739
hgdprs36038739
ensemblrs36038739
gopubmedrs36038739
geneviewrs36038739
scholarrs36038739
googlers36038739
pharmgkbrs36038739
gwascentralrs36038739
openSNPrs36038739
23andMers36038739
23andMe allrs36038739
SNP Nexus

SNPshotrs36038739
SNPdbers36038739
MSV3drs36038739
GWAS Ctlgrs36038739
Max Magnitude0
OMIM141900
Desc
Variant0067
Relatedalso
ClinVar
Risk rs36038739(C,T;C,T)
Alt rs36038739(C,T;C,T)
Reference rs36038739(G;G)
Significance Other
Disease HEMOGLOBIN DETROIT
Variation info
Gene HBB
CLNDBN HEMOGLOBIN DETROIT
Reversed 1
HGVS NC_000011.9:g.5247834C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016325.2,


[PMID 708768] Hemoglobin Detroit: beta95 (FG2) lysine leads to asparagine.