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rs587776827

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 3 Alpha-thalassemia allele carrier
(G;G) 0 common/normal


Make rs587776827(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position173471
GeneHBA2
is asnp
is mentioned by
dbSNPrs587776827
dbSNP (classic)rs587776827
ClinGenrs587776827
ebirs587776827
HLIrs587776827
Exacrs587776827
Gnomadrs587776827
Varsomers587776827
LitVarrs587776827
Maprs587776827
PheGenIrs587776827
Biobankrs587776827
1000 genomesrs587776827
hgdprs587776827
ensemblrs587776827
geneviewrs587776827
scholarrs587776827
googlers587776827
pharmgkbrs587776827
gwascentralrs587776827
openSNPrs587776827
23andMers587776827
23andMe allrs587776827
SNPshotrs587776827
SNPdbers587776827
MSV3drs587776827
GWAS Ctlgrs587776827
Max Magnitude3
ClinVar
Risk rs587776827(A;A)
Alt rs587776827(A;A)
Reference Rs587776827(G;G)
Significance Other
Disease HEMOGLOBIN CLINICO-MADRID Hemoglobin H disease
Variation info
Gene HBA2
CLNDBN HEMOGLOBIN CLINICO-MADRID Hemoglobin H disease, nondeletional
Reversed 0
HGVS NC_000016.9:g.223470G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016954.1, RCV000022607.4,