rs281864819

Orientation

plus

Stabilized

plus

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

Make rs281864819(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

172982

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs281864819
dbSNP (classic)	rs281864819
ClinGen	rs281864819
ebi	rs281864819
HLI	rs281864819
Exac	rs281864819
Gnomad	rs281864819
Varsome	rs281864819
LitVar	rs281864819
Map	rs281864819
PheGenI	rs281864819
Biobank	rs281864819
1000 genomes	rs281864819
hgdp	rs281864819
ensembl	rs281864819
geneview	rs281864819
scholar	rs281864819
google	rs281864819
pharmgkb	rs281864819
gwascentral	rs281864819
openSNP	rs281864819
23andMe	rs281864819
SNPshot	rs281864819
SNPdbe	rs281864819
MSV3d	rs281864819
GWAS Ctlg	rs281864819

Max Magnitude

3

ClinVar
Risk	rs281864819(A;A) rs281864819(C;C) rs281864819(T;T)
Alt	rs281864819(A;A) rs281864819(C;C) rs281864819(T;T)
Reference	Rs281864819(G;G)
Significance	Pathogenic
Disease	Alpha Thalassemia
Variation	info
Gene	HBA2
CLNDBN	alpha Thalassemia
Reversed	0
HGVS	NC_000016.9:g.222981G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016976.28,