rs121913304

Orientation

plus

Stabilized

plus

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

Make rs121913304(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

48381414

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs121913304
dbSNP (classic)	rs121913304
ClinGen	rs121913304
ebi	rs121913304
HLI	rs121913304
Exac	rs121913304
Gnomad	rs121913304
Varsome	rs121913304
LitVar	rs121913304
Map	rs121913304
PheGenI	rs121913304
Biobank	rs121913304
1000 genomes	rs121913304
hgdp	rs121913304
ensembl	rs121913304
geneview	rs121913304
scholar	rs121913304
google	rs121913304
pharmgkb	rs121913304
gwascentral	rs121913304
openSNP	rs121913304
23andMe	rs121913304
SNPshot	rs121913304
SNPdbe	rs121913304
MSV3d	rs121913304
GWAS Ctlg	rs121913304

Max Magnitude

6.8

OMIM	180200
Desc
Variant	0022
Related	also

ClinVar
Risk	rs121913304(T;T)
Alt	rs121913304(T;T)
Reference	Rs121913304(C;C)
Significance	Pathogenic
Disease	Retinoblastoma Neoplasm Hereditary cancer-predisposing syndrome
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma, trilateral Retinoblastoma Neoplasm Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.48955550C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013966.2, RCV000114734.1, RCV000430238.1, RCV000492084.1,