rs63750915

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(D;D)	0
(TATTTTCCCACCCTTAG;TATTTTCCCACCCTTAG)	0	common in clinvar

Make rs63750915(-;-)

Make rs63750915(-;TATTTTCCCACCCTTAG)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226800

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs63750915
dbSNP (classic)	rs63750915
ClinGen	rs63750915
ebi	rs63750915
HLI	rs63750915
Exac	rs63750915
Gnomad	rs63750915
Varsome	rs63750915
LitVar	rs63750915
Map	rs63750915
PheGenI	rs63750915
Biobank	rs63750915
1000 genomes	rs63750915
hgdp	rs63750915
ensembl	rs63750915
geneview	rs63750915
scholar	rs63750915
google	rs63750915
pharmgkb	rs63750915
gwascentral	rs63750915
openSNP	rs63750915
23andMe	rs63750915
SNPshot	rs63750915
SNPdbe	rs63750915
MSV3d	rs63750915
GWAS Ctlg	rs63750915

Max Magnitude

0

OMIM	141900
Desc
Variant	0351
Related	also

ClinVar
Risk
Alt
Reference	Rs63750915(TATTTTCCCACCCTTAG;TATTTTCCCACCCTTAG)
Significance	Pathogenic
Disease
Variation	info
Gene	HBB
CLNDBN
Reversed	1
HGVS	NC_000011.9:g.5248030_5248046delCTAAGGGTGGGAAAATA
CLNSRC
CLNACC

[PMID 3048433] Molecular basis and prenatal diagnosis of beta-thalassemia.