rs587776780

Orientation

plus

Stabilized

plus

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

Make rs587776780(C;C)

Make rs587776780(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48456351

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs587776780
dbSNP (classic)	rs587776780
ClinGen	rs587776780
ebi	rs587776780
HLI	rs587776780
Exac	rs587776780
Gnomad	rs587776780
Varsome	rs587776780
LitVar	rs587776780
Map	rs587776780
PheGenI	rs587776780
Biobank	rs587776780
1000 genomes	rs587776780
hgdp	rs587776780
ensembl	rs587776780
geneview	rs587776780
scholar	rs587776780
google	rs587776780
pharmgkb	rs587776780
gwascentral	rs587776780
openSNP	rs587776780
23andMe	rs587776780
SNPshot	rs587776780
SNPdbe	rs587776780
MSV3d	rs587776780
GWAS Ctlg	rs587776780

Max Magnitude

0

ClinVar
Risk	rs587776780(C;C)
Alt	rs587776780(C;C)
Reference	Rs587776780(T;T)
Significance	Pathogenic
Disease	Retinoblastoma
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma
Reversed	0
HGVS	NC_000013.10:g.49030487T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013945.4,