rs1057519637

Orientation

plus

Stabilized

plus

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

Make rs1057519637(-;-)

Make rs1057519637(-;AG)

Make rs1057519637(AG;AG)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

173006

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs1057519637
dbSNP (classic)	rs1057519637
ClinGen	rs1057519637
ebi	rs1057519637
HLI	rs1057519637
Exac	rs1057519637
Gnomad	rs1057519637
Varsome	rs1057519637
LitVar	rs1057519637
Map	rs1057519637
PheGenI	rs1057519637
Biobank	rs1057519637
1000 genomes	rs1057519637
hgdp	rs1057519637
ensembl	rs1057519637
geneview	rs1057519637
scholar	rs1057519637
google	rs1057519637
pharmgkb	rs1057519637
gwascentral	rs1057519637
openSNP	rs1057519637
23andMe	rs1057519637
SNPshot	rs1057519637
SNPdbe	rs1057519637
MSV3d	rs1057519637
GWAS Ctlg	rs1057519637

Max Magnitude

0

ClinVar
Risk	rs1057519637(-;-)
Alt	rs1057519637(-;-)
Reference	Rs1057519637(GA;GA)
Significance	Pathogenic
Disease	Alpha Thalassemia
Variation	info
Gene	HBA2
CLNDBN	alpha Thalassemia
Reversed	0
HGVS	NC_000016.9:g.223005_223006delAG
CLNSRC
CLNACC	RCV000417216.1,