rs281864894

Orientation

minus

Stabilized

minus

Make rs281864894(C;C)

Make rs281864894(C;T)

Make rs281864894(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226738

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs281864894
dbSNP (classic)	rs281864894
ClinGen	rs281864894
ebi	rs281864894
HLI	rs281864894
Exac	rs281864894
Gnomad	rs281864894
Varsome	rs281864894
LitVar	rs281864894
Map	rs281864894
PheGenI	rs281864894
Biobank	rs281864894
1000 genomes	rs281864894
hgdp	rs281864894
ensembl	rs281864894
geneview	rs281864894
scholar	rs281864894
google	rs281864894
pharmgkb	rs281864894
gwascentral	rs281864894
openSNP	rs281864894
23andMe	rs281864894
SNPshot	rs281864894
SNPdbe	rs281864894
MSV3d	rs281864894
GWAS Ctlg	rs281864894

Merged from

Rs33930476

Max Magnitude

0

[PMID 2079433] New results of hemoglobin variant structure determinations by fast atom bombardment mass spectrometry.

ClinVar
Risk	rs281864894(T;T)
Alt	rs281864894(T;T)
Reference	rs281864894(C;C)
Significance	Other
Disease	HEMOGLOBIN GRENOBLE
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN GRENOBLE
Reversed	1
HGVS	NC_000011.9:g.5247968G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016759.2,