rs33988732

Orientation

minus

Stabilized

minus

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

Make rs33988732(A;G)

Make rs33988732(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226720

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33988732
dbSNP (classic)	rs33988732
ClinGen	rs33988732
ebi	rs33988732
HLI	rs33988732
Exac	rs33988732
Gnomad	rs33988732
Varsome	rs33988732
LitVar	rs33988732
Map	rs33988732
PheGenI	rs33988732
Biobank	rs33988732
1000 genomes	rs33988732
hgdp	rs33988732
ensembl	rs33988732
geneview	rs33988732
scholar	rs33988732
google	rs33988732
pharmgkb	rs33988732
gwascentral	rs33988732
openSNP	rs33988732
23andMe	rs33988732
SNPshot	rs33988732
SNPdbe	rs33988732
MSV3d	rs33988732
GWAS Ctlg	rs33988732

Max Magnitude

0

OMIM	141900
Desc
Variant	0129
Related	also

ClinVar
Risk	rs33988732(C;C) rs33988732(G;G)
Alt	rs33988732(C;C) rs33988732(G;G)
Reference	Rs33988732(A;A)
Significance	Other
Disease	HEMOGLOBIN J (DALOA)
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN J (DALOA)
Reversed	1
HGVS	NC_000011.9:g.5247950T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016415.3,

[PMID 6292136] Hb J Daloa (beta 57 (E1) Asn replaced by Asp): a new variant found in Ivory Coast.