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rs1060503067

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503067(G;T)
Make rs1060503067(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position48459756
GeneRB1
is asnp
is mentioned by
dbSNPrs1060503067
dbSNP (old)rs1060503067
ClinGenrs1060503067
ebirs1060503067
HLIrs1060503067
Exacrs1060503067
Gnomadrs1060503067
Varsomers1060503067
Maprs1060503067
PheGenIrs1060503067
Biobankrs1060503067
1000 genomesrs1060503067
hgdprs1060503067
ensemblrs1060503067
gopubmedrs1060503067
geneviewrs1060503067
scholarrs1060503067
googlers1060503067
pharmgkbrs1060503067
gwascentralrs1060503067
openSNPrs1060503067
23andMers1060503067
23andMe allrs1060503067
SNPshotrs1060503067
SNPdbers1060503067
MSV3drs1060503067
GWAS Ctlgrs1060503067
Max Magnitude0
ClinVar
Risk rs1060503067(T;T)
Alt rs1060503067(T;T)
Reference Rs1060503067(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49033892G>T
CLNSRC
CLNACC RCV000470261.1,