rs137853293

Orientation

plus

Stabilized

plus

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

Make rs137853293(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

48465238

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs137853293
dbSNP (classic)	rs137853293
ClinGen	rs137853293
ebi	rs137853293
HLI	rs137853293
Exac	rs137853293
Gnomad	rs137853293
Varsome	rs137853293
LitVar	rs137853293
Map	rs137853293
PheGenI	rs137853293
Biobank	rs137853293
1000 genomes	rs137853293
hgdp	rs137853293
ensembl	rs137853293
geneview	rs137853293
scholar	rs137853293
google	rs137853293
pharmgkb	rs137853293
gwascentral	rs137853293
openSNP	rs137853293
23andMe	rs137853293
SNPshot	rs137853293
SNPdbe	rs137853293
MSV3d	rs137853293
GWAS Ctlg	rs137853293

Max Magnitude

6.8

OMIM	180200
Desc
Variant	0005
Related	also

ClinVar
Risk	rs137853293(T;T)
Alt	rs137853293(T;T)
Reference	Rs137853293(C;C)
Significance	Pathogenic
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.49039374C>T
CLNSRC	HGMD OMIM Allelic Variant
CLNACC	RCV000013948.3, RCV000078637.3, RCV000492108.1,