rs33956555

Orientation

minus

Stabilized

minus

Make rs33956555(C;C)

Make rs33956555(C;G)

Make rs33956555(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226798

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33956555
dbSNP (classic)	rs33956555
ClinGen	rs33956555
ebi	rs33956555
HLI	rs33956555
Exac	rs33956555
Gnomad	rs33956555
Varsome	rs33956555
LitVar	rs33956555
Map	rs33956555
PheGenI	rs33956555
Biobank	rs33956555
1000 genomes	rs33956555
hgdp	rs33956555
ensembl	rs33956555
geneview	rs33956555
scholar	rs33956555
google	rs33956555
pharmgkb	rs33956555
gwascentral	rs33956555
openSNP	rs33956555
23andMe	rs33956555
SNPshot	rs33956555
SNPdbe	rs33956555
MSV3d	rs33956555
GWAS Ctlg	rs33956555

Merged from

Rs111033584

Max Magnitude

0

[PMID 11976817] Characterization of a new hemoglobin variant: Hb Badalona (beta31[B13]Leu-->Val).

ClinVar
Risk	rs33956555(G;G) rs33956555(T;T)
Alt	rs33956555(G;G) rs33956555(T;T)
Reference	rs33956555(C;C)
Significance	Other
Disease	HEMOGLOBIN MUSCAT
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN MUSCAT
Reversed	1
HGVS	NC_000011.9:g.5248028G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016771.2,