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rs387906520

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906520(G;T)
Make rs387906520(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position48303724
GeneLINC00441, RB1
is asnp
is mentioned by
dbSNPrs387906520
ebirs387906520
HLIrs387906520
Exacrs387906520
Varsomers387906520
Maprs387906520
PheGenIrs387906520
hapmaprs387906520
1000 genomesrs387906520
hgdprs387906520
ensemblrs387906520
gopubmedrs387906520
geneviewrs387906520
scholarrs387906520
googlers387906520
pharmgkbrs387906520
gwascentralrs387906520
openSNPrs387906520
23andMers387906520
23andMe allrs387906520
SNP Nexus

SNPshotrs387906520
SNPdbers387906520
MSV3drs387906520
GWAS Ctlgrs387906520
Max Magnitude0
ClinVar
Risk rs387906520(T;T)
Alt rs387906520(T;T)
Reference rs387906520(G;G)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene LINC00441 RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48877860G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013960.2,