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rs376886420

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs376886420(A;G)
Make rs376886420(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position48453114
GeneRB1
is asnp
is mentioned by
dbSNPrs376886420
ebirs376886420
HLIrs376886420
Exacrs376886420
Varsomers376886420
Maprs376886420
PheGenIrs376886420
hapmaprs376886420
1000 genomesrs376886420
hgdprs376886420
ensemblrs376886420
gopubmedrs376886420
geneviewrs376886420
scholarrs376886420
googlers376886420
pharmgkbrs376886420
gwascentralrs376886420
openSNPrs376886420
23andMers376886420
23andMe allrs376886420
SNP Nexus

SNPshotrs376886420
SNPdbers376886420
MSV3drs376886420
GWAS Ctlgrs376886420
Max Magnitude0
ClinVar
Risk rs376886420(C,G;C,G)
Alt rs376886420(C,G;C,G)
Reference rs376886420(A;A)
Significance Probable-Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49027250A>C; NC_000013.10:g.49027250A>G
CLNSRC
CLNACC RCV000227413.1, RCV000238879.1,