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rs121913127

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913127(A;A)
Make rs121913127(A;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position177391
GeneHBA1
is asnp
is mentioned by
dbSNPrs121913127
ebirs121913127
HLIrs121913127
Exacrs121913127
Varsomers121913127
Maprs121913127
PheGenIrs121913127
hapmaprs121913127
1000 genomesrs121913127
hgdprs121913127
ensemblrs121913127
gopubmedrs121913127
geneviewrs121913127
scholarrs121913127
googlers121913127
pharmgkbrs121913127
gwascentralrs121913127
openSNPrs121913127
23andMers121913127
23andMe allrs121913127
SNP Nexus

SNPshotrs121913127
SNPdbers121913127
MSV3drs121913127
GWAS Ctlgrs121913127
Max Magnitude0
OMIM141800
Desc
Variant0020
Relatedalso
ClinVar
Risk rs121913127(A;A)
Alt rs121913127(A;A)
Reference rs121913127(C;C)
Significance Other
Disease HEMOGLOBIN CHICAGO
Variation info
Gene HBA1
CLNDBN HEMOGLOBIN CHICAGO
Reversed 0
HGVS NC_000016.9:g.227390C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017007.2,