rs587778861

Orientation

plus

Stabilized

plus

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

Make rs587778861(A;A)

Make rs587778861(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

48465033

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs587778861
dbSNP (classic)	rs587778861
ClinGen	rs587778861
ebi	rs587778861
HLI	rs587778861
Exac	rs587778861
Gnomad	rs587778861
Varsome	rs587778861
LitVar	rs587778861
Map	rs587778861
PheGenI	rs587778861
Biobank	rs587778861
1000 genomes	rs587778861
hgdp	rs587778861
ensembl	rs587778861
geneview	rs587778861
scholar	rs587778861
google	rs587778861
pharmgkb	rs587778861
gwascentral	rs587778861
openSNP	rs587778861
23andMe	rs587778861
SNPshot	rs587778861
SNPdbe	rs587778861
MSV3d	rs587778861
GWAS Ctlg	rs587778861

Max Magnitude

0

ClinVar
Risk	rs587778861(A;A) rs587778861(C;C)
Alt	rs587778861(A;A) rs587778861(C;C)
Reference	Rs587778861(T;T)
Significance	Pathogenic
Disease	Retinoblastoma
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma
Reversed	0
HGVS	NC_000013.10:g.49039169T>A
CLNSRC
CLNACC	RCV000114693.1,