rs587778826

Orientation

plus

Stabilized

plus

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

Make rs587778826(G;T)

Make rs587778826(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48347832

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs587778826
dbSNP (classic)	rs587778826
ClinGen	rs587778826
ebi	rs587778826
HLI	rs587778826
Exac	rs587778826
Gnomad	rs587778826
Varsome	rs587778826
LitVar	rs587778826
Map	rs587778826
PheGenI	rs587778826
Biobank	rs587778826
1000 genomes	rs587778826
hgdp	rs587778826
ensembl	rs587778826
geneview	rs587778826
scholar	rs587778826
google	rs587778826
pharmgkb	rs587778826
gwascentral	rs587778826
openSNP	rs587778826
23andMe	rs587778826
SNPshot	rs587778826
SNPdbe	rs587778826
MSV3d	rs587778826
GWAS Ctlg	rs587778826

Max Magnitude

0

ClinVar
Risk	rs587778826(T;T)
Alt	rs587778826(T;T)
Reference	Rs587778826(G;G)
Significance	Pathogenic
Disease	Retinoblastoma
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma
Reversed	0
HGVS	NC_000013.10:g.48921968G>T
CLNSRC
CLNACC	RCV000114706.1,