rs121913305

Orientation

plus

Stabilized

plus

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

Make rs121913305(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48453032

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs121913305
dbSNP (classic)	rs121913305
ClinGen	rs121913305
ebi	rs121913305
HLI	rs121913305
Exac	rs121913305
Gnomad	rs121913305
Varsome	rs121913305
LitVar	rs121913305
Map	rs121913305
PheGenI	rs121913305
Biobank	rs121913305
1000 genomes	rs121913305
hgdp	rs121913305
ensembl	rs121913305
geneview	rs121913305
scholar	rs121913305
google	rs121913305
pharmgkb	rs121913305
gwascentral	rs121913305
openSNP	rs121913305
23andMe	rs121913305
SNPshot	rs121913305
SNPdbe	rs121913305
MSV3d	rs121913305
GWAS Ctlg	rs121913305

Max Magnitude

6.8

ClinVar
Risk	rs121913305(T;T)
Alt	rs121913305(T;T)
Reference	Rs121913305(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.49027168C>T
CLNSRC
CLNACC	RCV000114677.2, RCV000492238.1,