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rs587776791

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Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776791(A;G)
Make rs587776791(G;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position48471962
GeneRB1
is asnp
is mentioned by
dbSNPrs587776791
ebirs587776791
HLIrs587776791
Exacrs587776791
Varsomers587776791
Maprs587776791
PheGenIrs587776791
hapmaprs587776791
1000 genomesrs587776791
hgdprs587776791
ensemblrs587776791
gopubmedrs587776791
geneviewrs587776791
scholarrs587776791
googlers587776791
pharmgkbrs587776791
gwascentralrs587776791
openSNPrs587776791
23andMers587776791
23andMe allrs587776791
SNP Nexus

SNPshotrs587776791
SNPdbers587776791
MSV3drs587776791
GWAS Ctlgrs587776791
Max Magnitude0
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,