rs63751425

Orientation

minus

Stabilized

minus

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

Make rs63751425(-;-)

Make rs63751425(-;A)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5225608

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs63751425
dbSNP (classic)	rs63751425
ClinGen	rs63751425
ebi	rs63751425
HLI	rs63751425
Exac	rs63751425
Gnomad	rs63751425
Varsome	rs63751425
LitVar	rs63751425
Map	rs63751425
PheGenI	rs63751425
Biobank	rs63751425
1000 genomes	rs63751425
hgdp	rs63751425
ensembl	rs63751425
geneview	rs63751425
scholar	rs63751425
google	rs63751425
pharmgkb	rs63751425
gwascentral	rs63751425
openSNP	rs63751425
23andMe	rs63751425
SNPshot	rs63751425
SNPdbe	rs63751425
MSV3d	rs63751425
GWAS Ctlg	rs63751425

Max Magnitude

0

OMIM	141900
Desc
Variant	0515
Related	also

ClinVar
Risk	rs63751425(-;-)
Alt	rs63751425(-;-)
Reference	Rs63751425(A;A)
Significance	Other
Disease	HEMOGLOBIN TRENTO
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN TRENTO
Reversed	1
HGVS	NC_000011.9:g.5246838delT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016871.2,

[PMID 12603089] Hb Trento: an elongated C-terminal beta chain due to a new frameshift mutation [beta144 (-A)].