rs587776786

Orientation

plus

Stabilized

plus

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

Make rs587776786(A;A)

Make rs587776786(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48464997

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs587776786
dbSNP (classic)	rs587776786
ClinGen	rs587776786
ebi	rs587776786
HLI	rs587776786
Exac	rs587776786
Gnomad	rs587776786
Varsome	rs587776786
LitVar	rs587776786
Map	rs587776786
PheGenI	rs587776786
Biobank	rs587776786
1000 genomes	rs587776786
hgdp	rs587776786
ensembl	rs587776786
geneview	rs587776786
scholar	rs587776786
google	rs587776786
pharmgkb	rs587776786
gwascentral	rs587776786
openSNP	rs587776786
23andMe	rs587776786
SNPshot	rs587776786
SNPdbe	rs587776786
MSV3d	rs587776786
GWAS Ctlg	rs587776786

Max Magnitude

0

ClinVar
Risk	rs587776786(A;A)
Alt	rs587776786(A;A)
Reference	Rs587776786(G;G)
Significance	Pathogenic
Disease	Retinoblastoma
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma
Reversed	0
HGVS	NC_000013.10:g.49039133G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013959.4,