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rs587776826

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACCAAGA;ACCAAGA) 0 common in clinvar
Make rs587776826(ACCAAGA;TACTTC)
Make rs587776826(TACTTC;TACTTC)
ReferenceGRCh38 38.1/142
Chromosome16
Position173147
GeneHBA2
is asnp
is mentioned by
dbSNPrs587776826
ebirs587776826
HLIrs587776826
Exacrs587776826
Varsomers587776826
Maprs587776826
PheGenIrs587776826
hapmaprs587776826
1000 genomesrs587776826
hgdprs587776826
ensemblrs587776826
gopubmedrs587776826
geneviewrs587776826
scholarrs587776826
googlers587776826
pharmgkbrs587776826
gwascentralrs587776826
openSNPrs587776826
23andMers587776826
23andMe allrs587776826
SNP Nexus

SNPshotrs587776826
SNPdbers587776826
MSV3drs587776826
GWAS Ctlgrs587776826
Max Magnitude0
ClinVar
Risk rs587776826(TACTTC;TACTTC)
Alt rs587776826(TACTTC;TACTTC)
Reference rs587776826(ACCAAGA;ACCAAGA)
Significance Pathogenic
Disease Alpha trait thalassemia
Variation info
Gene HBA2
CLNDBN Alpha trait thalassemia
Reversed 0
HGVS NC_000016.9:g.223146_223152delACCAAGAinsTACTTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000016943.26,