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rs41515649

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41515649(A;A)
Make rs41515649(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position173216
GeneHBA2
is asnp
is mentioned by
dbSNPrs41515649
ebirs41515649
HLIrs41515649
Exacrs41515649
Varsomers41515649
Maprs41515649
PheGenIrs41515649
hapmaprs41515649
1000 genomesrs41515649
hgdprs41515649
ensemblrs41515649
gopubmedrs41515649
geneviewrs41515649
scholarrs41515649
googlers41515649
pharmgkbrs41515649
gwascentralrs41515649
openSNPrs41515649
23andMers41515649
23andMe allrs41515649
SNP Nexus

SNPshotrs41515649
SNPdbers41515649
MSV3drs41515649
GWAS Ctlgrs41515649
Max Magnitude0
OMIM141850
Desc
Variant0006
Relatedalso


ClinVar
Risk rs41515649(A;A)
Alt rs41515649(A;A)
Reference rs41515649(G;G)
Significance Other
Disease HEMOGLOBIN EVANS
Variation info
Gene HBA2
CLNDBN HEMOGLOBIN EVANS
Reversed 0
HGVS NC_000016.9:g.223215G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016898.1,



[PMID 2606724] Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia.