rs63749858

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs63749858(-;-)

Make rs63749858(-;A)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5225611

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs63749858
dbSNP (classic)	rs63749858
ClinGen	rs63749858
ebi	rs63749858
HLI	rs63749858
Exac	rs63749858
Gnomad	rs63749858
Varsome	rs63749858
LitVar	rs63749858
Map	rs63749858
PheGenI	rs63749858
Biobank	rs63749858
1000 genomes	rs63749858
hgdp	rs63749858
ensembl	rs63749858
geneview	rs63749858
scholar	rs63749858
google	rs63749858
pharmgkb	rs63749858
gwascentral	rs63749858
openSNP	rs63749858
23andMe	rs63749858
SNPshot	rs63749858
SNPdbe	rs63749858
MSV3d	rs63749858
GWAS Ctlg	rs63749858

Max Magnitude

0

OMIM	141900
Desc
Variant	0255
Related	also

ClinVar
Risk	rs63749858(-;-)
Alt	rs63749858(-;-)
Reference	Rs63749858(A;A)
Significance	Other
Disease	HEMOGLOBIN SAVERNE
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN SAVERNE
Reversed	1
HGVS	NC_000011.9:g.5246841delT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016588.3,

[PMID 3170236] Hemoglobin Saverne: a new variant with elongated beta chains: structural and functional properties.