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rs587776786

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776786(A;A)
Make rs587776786(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48464997
GeneRB1
is asnp
is mentioned by
dbSNPrs587776786
ebirs587776786
HLIrs587776786
Exacrs587776786
Varsomers587776786
Maprs587776786
PheGenIrs587776786
hapmaprs587776786
1000 genomesrs587776786
hgdprs587776786
ensemblrs587776786
gopubmedrs587776786
geneviewrs587776786
scholarrs587776786
googlers587776786
pharmgkbrs587776786
gwascentralrs587776786
openSNPrs587776786
23andMers587776786
23andMe allrs587776786
SNP Nexus

SNPshotrs587776786
SNPdbers587776786
MSV3drs587776786
GWAS Ctlgrs587776786
Max Magnitude0
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,