rs267607297

Orientation

minus

Stabilized

minus

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

Make rs267607297(-;-)

Make rs267607297(-;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226784

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs267607297
dbSNP (classic)	rs267607297
ClinGen	rs267607297
ebi	rs267607297
HLI	rs267607297
Exac	rs267607297
Gnomad	rs267607297
Varsome	rs267607297
LitVar	rs267607297
Map	rs267607297
PheGenI	rs267607297
Biobank	rs267607297
1000 genomes	rs267607297
hgdp	rs267607297
ensembl	rs267607297
geneview	rs267607297
scholar	rs267607297
google	rs267607297
pharmgkb	rs267607297
gwascentral	rs267607297
openSNP	rs267607297
23andMe	rs267607297
SNPshot	rs267607297
SNPdbe	rs267607297
MSV3d	rs267607297
GWAS Ctlg	rs267607297

Max Magnitude

0

ClinVar
Risk	rs267607297(-;-)
Alt	rs267607297(-;-)
Reference	Rs267607297(C;C)
Significance	Pathogenic
Disease	beta^0^ Thalassemia
Variation	info
Gene	HBB
CLNDBN	beta^0^ Thalassemia
Reversed	1
HGVS	NC_000011.9:g.5248014delG
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000016680.26,

[PMID 2736244] Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia major.