rs33953406

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in complete genomics

Make rs33953406(A;C)

Make rs33953406(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5225645

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33953406
dbSNP (classic)	rs33953406
ClinGen	rs33953406
ebi	rs33953406
HLI	rs33953406
Exac	rs33953406
Gnomad	rs33953406
Varsome	rs33953406
LitVar	rs33953406
Map	rs33953406
PheGenI	rs33953406
Biobank	rs33953406
1000 genomes	rs33953406
hgdp	rs33953406
ensembl	rs33953406
geneview	rs33953406
scholar	rs33953406
google	rs33953406
pharmgkb	rs33953406
gwascentral	rs33953406
openSNP	rs33953406
23andMe	rs33953406
SNPshot	rs33953406
SNPdbe	rs33953406
MSV3d	rs33953406
GWAS Ctlg	rs33953406

Max Magnitude

0

OMIM	141900
Desc
Variant	0143
Related	also

ClinVar
Risk	rs33953406(C;C) rs33953406(G;G) rs33953406(T;T)
Alt	rs33953406(C;C) rs33953406(G;G) rs33953406(T;T)
Reference	Rs33953406(A;A)
Significance	Other
Disease	HEMOGLOBIN K (WOOLWICH)
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN K (WOOLWICH)
Reversed	1
HGVS	NC_000011.9:g.5246875T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016431.2,

[PMID 4999133] Haemoglobin K Woolwich (alpha 2, beta 2 132 lysine leads to glutamine) in Ghana.

[PMID 6249934] Haemoglobin K Woolwich: a study of the family of a homozygote.