rs587778833

Orientation

plus

Stabilized

plus

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

Make rs587778833(C;T)

Make rs587778833(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48456298

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs587778833
dbSNP (classic)	rs587778833
ClinGen	rs587778833
ebi	rs587778833
HLI	rs587778833
Exac	rs587778833
Gnomad	rs587778833
Varsome	rs587778833
LitVar	rs587778833
Map	rs587778833
PheGenI	rs587778833
Biobank	rs587778833
1000 genomes	rs587778833
hgdp	rs587778833
ensembl	rs587778833
geneview	rs587778833
scholar	rs587778833
google	rs587778833
pharmgkb	rs587778833
gwascentral	rs587778833
openSNP	rs587778833
23andMe	rs587778833
SNPshot	rs587778833
SNPdbe	rs587778833
MSV3d	rs587778833
GWAS Ctlg	rs587778833

Max Magnitude

0

ClinVar
Risk	rs587778833(T;T)
Alt	rs587778833(T;T)
Reference	Rs587778833(C;C)
Significance	Pathogenic
Disease	Retinoblastoma
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma
Reversed	0
HGVS	NC_000013.10:g.49030434C>T
CLNSRC
CLNACC	RCV000114680.1,