rs121913296

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(G;T)	6.8	Retinoblastoma (predicted)

Make rs121913296(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48345108

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs121913296
dbSNP (classic)	rs121913296
ClinGen	rs121913296
ebi	rs121913296
HLI	rs121913296
Exac	rs121913296
Gnomad	rs121913296
Varsome	rs121913296
LitVar	rs121913296
Map	rs121913296
PheGenI	rs121913296
Biobank	rs121913296
1000 genomes	rs121913296
hgdp	rs121913296
ensembl	rs121913296
geneview	rs121913296
scholar	rs121913296
google	rs121913296
pharmgkb	rs121913296
gwascentral	rs121913296
openSNP	rs121913296
23andMe	rs121913296
SNPshot	rs121913296
SNPdbe	rs121913296
MSV3d	rs121913296
GWAS Ctlg	rs121913296

Max Magnitude

6.8

ClinVar
Risk	rs121913296(T;T)
Alt	rs121913296(T;T)
Reference	Rs121913296(G;G)
Significance	Pathogenic
Disease	Retinoblastoma Neoplasm
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma Neoplasm
Reversed	0
HGVS	NC_000013.10:g.48919244G>T
CLNSRC
CLNACC	RCV000114702.1, RCV000427414.1,