rs33974277

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics
(GG;GG)	0	common in clinvar

Make rs33974277(A;A)

Make rs33974277(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226934

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33974277
dbSNP (classic)	rs33974277
ClinGen	rs33974277
ebi	rs33974277
HLI	rs33974277
Exac	rs33974277
Gnomad	rs33974277
Varsome	rs33974277
LitVar	rs33974277
Map	rs33974277
PheGenI	rs33974277
Biobank	rs33974277
1000 genomes	rs33974277
hgdp	rs33974277
ensembl	rs33974277
geneview	rs33974277
scholar	rs33974277
google	rs33974277
pharmgkb	rs33974277
gwascentral	rs33974277
openSNP	rs33974277
23andMe	rs33974277
SNPshot	rs33974277
SNPdbe	rs33974277
MSV3d	rs33974277
GWAS Ctlg	rs33974277

Merged from

Rs121909831

Max Magnitude

0

OMIM	141900
Desc
Variant	0526
Related	also

ClinVar
Risk	rs33974277(A;A)
Alt	rs33974277(A;A)
Reference	Rs33974277(G;G)
Significance	Other
Disease	HEMOGLOBIN TIZI-OUZOU
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN TIZI-OUZOU
Reversed	1
HGVS	NC_000011.9:g.5248164C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016882.2,

[PMID 15481887] Two new beta-chain variants: Hb Tripoli [beta26(B8)Glu-->Ala] and Hb Tizi-Ouzou [beta29(B11)Gly-->Ser].