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rs587776828

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;A) 3 Alpha-thalassemia allele carrier
(A;A) 0 common in clinvar


Make rs587776828(-;-)
ReferenceGRCh38 38.1/142
Chromosome16
Position172913
GeneHBA2
is asnp
is mentioned by
dbSNPrs587776828
ebirs587776828
HLIrs587776828
Exacrs587776828
Varsomers587776828
Maprs587776828
PheGenIrs587776828
hapmaprs587776828
1000 genomesrs587776828
hgdprs587776828
ensemblrs587776828
gopubmedrs587776828
geneviewrs587776828
scholarrs587776828
googlers587776828
pharmgkbrs587776828
gwascentralrs587776828
openSNPrs587776828
23andMers587776828
23andMe allrs587776828
SNP Nexus

SNPshotrs587776828
SNPdbers587776828
MSV3drs587776828
GWAS Ctlgrs587776828
Max Magnitude3
ClinVar
Risk rs587776828(;)
Alt rs587776828(;)
Reference rs587776828(A;A)
Significance Pathogenic
Disease Alpha-thalassemia
Variation info
Gene HBA2
CLNDBN Alpha-thalassemia, Hmong type
Reversed 0
HGVS NC_000016.9:g.222912delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000016985.22,