rs1060339

Orientation

plus

Stabilized

plus

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

Make rs1060339(A;A)

Make rs1060339(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

177040

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs1060339
dbSNP (classic)	rs1060339
ClinGen	rs1060339
ebi	rs1060339
HLI	rs1060339
Exac	rs1060339
Gnomad	rs1060339
Varsome	rs1060339
LitVar	rs1060339
Map	rs1060339
PheGenI	rs1060339
Biobank	rs1060339
1000 genomes	rs1060339
hgdp	rs1060339
ensembl	rs1060339
geneview	rs1060339
scholar	rs1060339
google	rs1060339
pharmgkb	rs1060339
gwascentral	rs1060339
openSNP	rs1060339
23andMe	rs1060339
SNPshot	rs1060339
SNPdbe	rs1060339
MSV3d	rs1060339
GWAS Ctlg	rs1060339

Max Magnitude

0

ClinVar
Risk	rs1060339(A;A) rs1060339(G;G)
Alt	rs1060339(A;A) rs1060339(G;G)
Reference	Rs1060339(C;C)
Significance	Pathogenic
Disease	Alpha Thalassemia
Variation	info
Gene	HBA1
CLNDBN	alpha Thalassemia
Reversed	0
HGVS	NC_000016.9:g.227039C>A
CLNSRC
CLNACC	RCV000417227.1,