rs587776827

Orientation

plus

Stabilized

plus

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

Make rs587776827(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

173471

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs587776827
dbSNP (classic)	rs587776827
ClinGen	rs587776827
ebi	rs587776827
HLI	rs587776827
Exac	rs587776827
Gnomad	rs587776827
Varsome	rs587776827
LitVar	rs587776827
Map	rs587776827
PheGenI	rs587776827
Biobank	rs587776827
1000 genomes	rs587776827
hgdp	rs587776827
ensembl	rs587776827
geneview	rs587776827
scholar	rs587776827
google	rs587776827
pharmgkb	rs587776827
gwascentral	rs587776827
openSNP	rs587776827
23andMe	rs587776827
SNPshot	rs587776827
SNPdbe	rs587776827
MSV3d	rs587776827
GWAS Ctlg	rs587776827

Max Magnitude

3

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,