rs63751457

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	Alpha-thalassemia allele carrier

Make rs63751457(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

172981

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs63751457
dbSNP (classic)	rs63751457
ClinGen	rs63751457
ebi	rs63751457
HLI	rs63751457
Exac	rs63751457
Gnomad	rs63751457
Varsome	rs63751457
LitVar	rs63751457
Map	rs63751457
PheGenI	rs63751457
Biobank	rs63751457
1000 genomes	rs63751457
hgdp	rs63751457
ensembl	rs63751457
geneview	rs63751457
scholar	rs63751457
google	rs63751457
pharmgkb	rs63751457
gwascentral	rs63751457
openSNP	rs63751457
23andMe	rs63751457
SNPshot	rs63751457
SNPdbe	rs63751457
MSV3d	rs63751457
GWAS Ctlg	rs63751457

Max Magnitude

3

OMIM	141850
Desc
Variant	0064
Related	also

ClinVar
Risk	rs63751457(T;T)
Alt	rs63751457(T;T)
Reference	Rs63751457(C;C)
Significance	Pathogenic
Disease	Alpha plus thalassemia
Variation	info
Gene	HBA2
CLNDBN	Alpha plus thalassemia
Reversed	0
HGVS	NC_000016.9:g.222980C>T
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000016977.26,