rs587778832

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(I;I)	0	common genotype
(TT;TT)	0	common in clinvar

Make rs587778832(-;-)

Make rs587778832(-;TT)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48380199

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs587778832
dbSNP (classic)	rs587778832
ClinGen	rs587778832
ebi	rs587778832
HLI	rs587778832
Exac	rs587778832
Gnomad	rs587778832
Varsome	rs587778832
LitVar	rs587778832
Map	rs587778832
PheGenI	rs587778832
Biobank	rs587778832
1000 genomes	rs587778832
hgdp	rs587778832
ensembl	rs587778832
geneview	rs587778832
scholar	rs587778832
google	rs587778832
pharmgkb	rs587778832
gwascentral	rs587778832
openSNP	rs587778832
23andMe	rs587778832
SNPshot	rs587778832
SNPdbe	rs587778832
MSV3d	rs587778832
GWAS Ctlg	rs587778832

Max Magnitude

0

ClinVar
Risk	rs587778832(-;-)
Alt	rs587778832(-;-)
Reference	Rs587778832(TT;TT)
Significance	Pathogenic
Disease	Retinoblastoma
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma
Reversed	0
HGVS	NC_000013.10:g.48954335_48954336delTT
CLNSRC
CLNACC	RCV000114731.1,