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rs41393644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs41393644(A;C)
Make rs41393644(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position173591
GeneHBA2
is asnp
is mentioned by
dbSNPrs41393644
ebirs41393644
HLIrs41393644
Exacrs41393644
Varsomers41393644
Maprs41393644
PheGenIrs41393644
hapmaprs41393644
1000 genomesrs41393644
hgdprs41393644
ensemblrs41393644
gopubmedrs41393644
geneviewrs41393644
scholarrs41393644
googlers41393644
pharmgkbrs41393644
gwascentralrs41393644
openSNPrs41393644
23andMers41393644
23andMe allrs41393644
SNP Nexus

SNPshotrs41393644
SNPdbers41393644
MSV3drs41393644
GWAS Ctlgrs41393644
Max Magnitude0
OMIM141850
Desc
Variant0059
Relatedalso


ClinVar
Risk rs41393644(C;C)
Alt rs41393644(C;C)
Reference rs41393644(A;A)
Significance Other
Disease HEMOGLOBIN FUKUI
Variation info
Gene HBA2
CLNDBN HEMOGLOBIN FUKUI
Reversed 0
HGVS NC_000016.9:g.223590A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016971.1,



[PMID 12779274] A new hemoglobin variant, Hb Fukui [alpha139(HC1)Lys --> Asn (AAA --> AAC) (alpha2)].