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rs41466346

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs41466346(C;G)
Make rs41466346(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position173270
GeneHBA2
is asnp
is mentioned by
dbSNPrs41466346
ebirs41466346
HLIrs41466346
Exacrs41466346
Varsomers41466346
Maprs41466346
PheGenIrs41466346
hapmaprs41466346
1000 genomesrs41466346
hgdprs41466346
ensemblrs41466346
gopubmedrs41466346
geneviewrs41466346
scholarrs41466346
googlers41466346
pharmgkbrs41466346
gwascentralrs41466346
openSNPrs41466346
23andMers41466346
23andMe allrs41466346
SNP Nexus

SNPshotrs41466346
SNPdbers41466346
MSV3drs41466346
GWAS Ctlgrs41466346
Max Magnitude0
OMIM141850
Desc
Variant0035
Relatedalso


ClinVar
Risk rs41466346(G;G)
Alt rs41466346(G;G)
Reference rs41466346(C;C)
Significance Other
Disease HEMOGLOBIN CONAKRY
Variation info
Gene HBA2
CLNDBN HEMOGLOBIN CONAKRY
Reversed 0
HGVS NC_000016.9:g.223269C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016946.1,



[PMID 9886305] A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha2 globin gene variant (Hb Conakry).