rs587776826

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(ACCAAGA;ACCAAGA)	0	common in clinvar

Make rs587776826(ACCAAGA;TACTTC)

Make rs587776826(TACTTC;TACTTC)

Reference

GRCh38 38.1/142

Chromosome

16

Position

173147

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs587776826
dbSNP (classic)	rs587776826
ClinGen	rs587776826
ebi	rs587776826
HLI	rs587776826
Exac	rs587776826
Gnomad	rs587776826
Varsome	rs587776826
LitVar	rs587776826
Map	rs587776826
PheGenI	rs587776826
Biobank	rs587776826
1000 genomes	rs587776826
hgdp	rs587776826
ensembl	rs587776826
geneview	rs587776826
scholar	rs587776826
google	rs587776826
pharmgkb	rs587776826
gwascentral	rs587776826
openSNP	rs587776826
23andMe	rs587776826
SNPshot	rs587776826
SNPdbe	rs587776826
MSV3d	rs587776826
GWAS Ctlg	rs587776826

Max Magnitude

0

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	RCV000016943.28,