rs587778841

Orientation

plus

Stabilized

plus

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

Make rs587778841(-;-)

Make rs587778841(-;TGCT)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48345137

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs587778841
dbSNP (classic)	rs587778841
ClinGen	rs587778841
ebi	rs587778841
HLI	rs587778841
Exac	rs587778841
Gnomad	rs587778841
Varsome	rs587778841
LitVar	rs587778841
Map	rs587778841
PheGenI	rs587778841
Biobank	rs587778841
1000 genomes	rs587778841
hgdp	rs587778841
ensembl	rs587778841
geneview	rs587778841
scholar	rs587778841
google	rs587778841
pharmgkb	rs587778841
gwascentral	rs587778841
openSNP	rs587778841
23andMe	rs587778841
SNPshot	rs587778841
SNPdbe	rs587778841
MSV3d	rs587778841
GWAS Ctlg	rs587778841

Max Magnitude

0

ClinVar
Risk	rs587778841(-;-)
Alt	rs587778841(-;-)
Reference	Rs587778841(TGCT;TGCT)
Significance	Pathogenic
Disease	Retinoblastoma
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma
Reversed	0
HGVS	NC_000013.10:g.48919273_48919276delTGCT
CLNSRC
CLNACC	RCV000114703.1,