rs587776791

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	6.8	Retinoblastoma (predicted)

Make rs587776791(G;G)

Reference

GRCh38 38.1/142

Chromosome

13

Position

48471962

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs587776791
dbSNP (classic)	rs587776791
ClinGen	rs587776791
ebi	rs587776791
HLI	rs587776791
Exac	rs587776791
Gnomad	rs587776791
Varsome	rs587776791
LitVar	rs587776791
Map	rs587776791
PheGenI	rs587776791
Biobank	rs587776791
1000 genomes	rs587776791
hgdp	rs587776791
ensembl	rs587776791
geneview	rs587776791
scholar	rs587776791
google	rs587776791
pharmgkb	rs587776791
gwascentral	rs587776791
openSNP	rs587776791
23andMe	rs587776791
SNPshot	rs587776791
SNPdbe	rs587776791
MSV3d	rs587776791
GWAS Ctlg	rs587776791

Max Magnitude

6.8

ClinVar
Risk	rs587776791(G;G)
Alt	rs587776791(G;G)
Reference	Rs587776791(A;A)
Significance	Pathogenic
Disease	Retinoblastoma
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma
Reversed	0
HGVS	NC_000013.10:g.49046098A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013972.2,