rs121913302

Orientation

plus

Stabilized

plus

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

Make rs121913302(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48379624

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs121913302
dbSNP (classic)	rs121913302
ClinGen	rs121913302
ebi	rs121913302
HLI	rs121913302
Exac	rs121913302
Gnomad	rs121913302
Varsome	rs121913302
LitVar	rs121913302
Map	rs121913302
PheGenI	rs121913302
Biobank	rs121913302
1000 genomes	rs121913302
hgdp	rs121913302
ensembl	rs121913302
geneview	rs121913302
scholar	rs121913302
google	rs121913302
pharmgkb	rs121913302
gwascentral	rs121913302
openSNP	rs121913302
23andMe	rs121913302
SNPshot	rs121913302
SNPdbe	rs121913302
MSV3d	rs121913302
GWAS Ctlg	rs121913302

Max Magnitude

6.8

ClinVar
Risk	rs121913302(T;T)
Alt	rs121913302(T;T)
Reference	Rs121913302(C;C)
Significance	Other
Disease	Retinoblastoma not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.48953760C>T
CLNSRC
CLNACC	RCV000114729.2, RCV000486601.1, RCV000492246.1,