rs33916541

Orientation

minus

Stabilized

minus

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

Make rs33916541(C;C)

Make rs33916541(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226669

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33916541
dbSNP (classic)	rs33916541
ClinGen	rs33916541
ebi	rs33916541
HLI	rs33916541
Exac	rs33916541
Gnomad	rs33916541
Varsome	rs33916541
LitVar	rs33916541
Map	rs33916541
PheGenI	rs33916541
Biobank	rs33916541
1000 genomes	rs33916541
hgdp	rs33916541
ensembl	rs33916541
geneview	rs33916541
scholar	rs33916541
google	rs33916541
pharmgkb	rs33916541
gwascentral	rs33916541
openSNP	rs33916541
23andMe	rs33916541
SNPshot	rs33916541
SNPdbe	rs33916541
MSV3d	rs33916541
GWAS Ctlg	rs33916541

Merged from

Rs121909804

Max Magnitude

0

OMIM	141900
Desc
Variant	0001
Related	also

ClinVar
Risk	rs33916541(A;A) rs33916541(C;C)
Alt	rs33916541(A;A) rs33916541(C;C)
Reference	Rs33916541(G;G)
Significance	Other
Disease	HEMOGLOBIN AALBORG
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN AALBORG
Reversed	1
HGVS	NC_000011.9:g.5247899C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016242.2,

[PMID 2272837] Characterization of Hb Aalborg, a new unstable hemoglobin variant, by fast atom bombardment mass spectrometry.