rs587778848

Orientation

plus

Stabilized

plus

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

Make rs587778848(C;C)

Make rs587778848(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48380215

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs587778848
dbSNP (classic)	rs587778848
ClinGen	rs587778848
ebi	rs587778848
HLI	rs587778848
Exac	rs587778848
Gnomad	rs587778848
Varsome	rs587778848
LitVar	rs587778848
Map	rs587778848
PheGenI	rs587778848
Biobank	rs587778848
1000 genomes	rs587778848
hgdp	rs587778848
ensembl	rs587778848
geneview	rs587778848
scholar	rs587778848
google	rs587778848
pharmgkb	rs587778848
gwascentral	rs587778848
openSNP	rs587778848
23andMe	rs587778848
SNPshot	rs587778848
SNPdbe	rs587778848
MSV3d	rs587778848
GWAS Ctlg	rs587778848

Max Magnitude

0

ClinVar
Risk	rs587778848(C;C)
Alt	rs587778848(C;C)
Reference	Rs587778848(T;T)
Significance	Pathogenic
Disease	Retinoblastoma not specified
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma not specified
Reversed	0
HGVS	NC_000013.10:g.48954351T>C
CLNSRC
CLNACC	RCV000114732.1, RCV000273920.1,