Rs11548605

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in complete genomics
Make rs11548605(A;A)
Make rs11548605(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position176781
GeneHBA1
is asnp
is mentioned by
dbSNPrs11548605
PheGenIrs11548605
nextbiors11548605
hapmaprs11548605
1000 genomesrs11548605
hgdprs11548605
ensemblrs11548605
gopubmedrs11548605
geneviewrs11548605
scholarrs11548605
googlers11548605
pharmgkbrs11548605
gwascentralrs11548605
openSNPrs11548605
23andMers11548605
23andMe allrs11548605
SNP Nexus

SNPshotrs11548605
SNPdbers11548605
MSV3drs11548605
Max Magnitude0
OMIM141800
Desc
Variant0068
Relatedalso
ClinVar
Risk rs11548605(A,T;A,T)
Alt rs11548605(A,T;A,T)
Reference rs11548605(C;C)
Significance Other
Disease HEMOGLOBIN J (NYANZA)
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN J (NYANZA)
Reversed 0
HGVS NC_000016.9:g.226780C>A
CLNSRC HBVAR OMIM Allelic Variant
CLNACC RCV000017067.1,


[PMID 4719146] Haemoglobin J Nyanza: 21 (B2) Ala-Asp.