rs121913300

Orientation

plus

Stabilized

plus

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

Make rs121913300(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48367512

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs121913300
dbSNP (classic)	rs121913300
ClinGen	rs121913300
ebi	rs121913300
HLI	rs121913300
Exac	rs121913300
Gnomad	rs121913300
Varsome	rs121913300
LitVar	rs121913300
Map	rs121913300
PheGenI	rs121913300
Biobank	rs121913300
1000 genomes	rs121913300
hgdp	rs121913300
ensembl	rs121913300
geneview	rs121913300
scholar	rs121913300
google	rs121913300
pharmgkb	rs121913300
gwascentral	rs121913300
openSNP	rs121913300
23andMe	rs121913300
SNPshot	rs121913300
SNPdbe	rs121913300
MSV3d	rs121913300
GWAS Ctlg	rs121913300

Max Magnitude

6.8

ClinVar
Risk	rs121913300(G;G) rs121913300(T;T)
Alt	rs121913300(G;G) rs121913300(T;T)
Reference	Rs121913300(C;C)
Significance	Other
Disease	Retinoblastoma Hereditary cancer-predisposing syndrome
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.48941648C>T
CLNSRC
CLNACC	RCV000114716.2, RCV000492534.1,