rs1060503088

Orientation

plus

Stabilized

plus

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

Make rs1060503088(G;G)

Make rs1060503088(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

48452981

Gene

RB1

is a	snp
is	mentioned by
dbSNP	rs1060503088
dbSNP (classic)	rs1060503088
ClinGen	rs1060503088
ebi	rs1060503088
HLI	rs1060503088
Exac	rs1060503088
Gnomad	rs1060503088
Varsome	rs1060503088
LitVar	rs1060503088
Map	rs1060503088
PheGenI	rs1060503088
Biobank	rs1060503088
1000 genomes	rs1060503088
hgdp	rs1060503088
ensembl	rs1060503088
geneview	rs1060503088
scholar	rs1060503088
google	rs1060503088
pharmgkb	rs1060503088
gwascentral	rs1060503088
openSNP	rs1060503088
23andMe	rs1060503088
SNPshot	rs1060503088
SNPdbe	rs1060503088
MSV3d	rs1060503088
GWAS Ctlg	rs1060503088

Max Magnitude

0

ClinVar
Risk	rs1060503088(G;G)
Alt	rs1060503088(G;G)
Reference	Rs1060503088(T;T)
Significance	Pathogenic
Disease	Retinoblastoma
Variation	info
Gene	RB1
CLNDBN	Retinoblastoma
Reversed	0
HGVS	NC_000013.10:g.49027117T>G
CLNSRC
CLNACC	RCV000471747.1,