rs398123332

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs398123332(-;T)

Make rs398123332(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

48381333

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs398123332
dbSNP (classic)	rs398123332
ClinGen	rs398123332
ebi	rs398123332
HLI	rs398123332
Exac	rs398123332
Gnomad	rs398123332
Varsome	rs398123332
LitVar	rs398123332
Map	rs398123332
PheGenI	rs398123332
Biobank	rs398123332
1000 genomes	rs398123332
hgdp	rs398123332
ensembl	rs398123332
geneview	rs398123332
scholar	rs398123332
google	rs398123332
pharmgkb	rs398123332
gwascentral	rs398123332
openSNP	rs398123332
23andMe	rs398123332
SNPshot	rs398123332
SNPdbe	rs398123332
MSV3d	rs398123332
GWAS Ctlg	rs398123332

Max Magnitude

0

ClinVar
Risk	rs398123332(T;T)
Alt	rs398123332(T;T)
Reference	Rs398123332(-;-)
Significance	Pathogenic
Disease	not provided Retinoblastoma
Variation	info
Gene	RB1
CLNDBN	not provided Retinoblastoma
Reversed	0
HGVS	NC_000013.10:g.48955469dupT
CLNSRC	HGMD
CLNACC	RCV000078634.3, RCV000175134.1,