rs121913303

Orientation

plus

Stabilized

plus

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

Make rs121913303(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48381402

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs121913303
dbSNP (classic)	rs121913303
ClinGen	rs121913303
ebi	rs121913303
HLI	rs121913303
Exac	rs121913303
Gnomad	rs121913303
Varsome	rs121913303
LitVar	rs121913303
Map	rs121913303
PheGenI	rs121913303
Biobank	rs121913303
1000 genomes	rs121913303
hgdp	rs121913303
ensembl	rs121913303
geneview	rs121913303
scholar	rs121913303
google	rs121913303
pharmgkb	rs121913303
gwascentral	rs121913303
openSNP	rs121913303
23andMe	rs121913303
SNPshot	rs121913303
SNPdbe	rs121913303
MSV3d	rs121913303
GWAS Ctlg	rs121913303

Max Magnitude

6.8

ClinVar
Risk	rs121913303(T;T)
Alt	rs121913303(T;T)
Reference	Rs121913303(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.48955538C>T
CLNSRC
CLNACC	RCV000114733.2, RCV000492730.1,