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rs727504121

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504121(-;-)
Make rs727504121(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position48373468
GeneRB1
is asnp
is mentioned by
dbSNPrs727504121
ebirs727504121
HLIrs727504121
Exacrs727504121
Varsomers727504121
Maprs727504121
PheGenIrs727504121
hapmaprs727504121
1000 genomesrs727504121
hgdprs727504121
ensemblrs727504121
gopubmedrs727504121
geneviewrs727504121
scholarrs727504121
googlers727504121
pharmgkbrs727504121
gwascentralrs727504121
openSNPrs727504121
23andMers727504121
23andMe allrs727504121
SNP Nexus

SNPshotrs727504121
SNPdbers727504121
MSV3drs727504121
GWAS Ctlgrs727504121
Max Magnitude0
ClinVar
Risk rs727504121(;)
Alt rs727504121(;)
Reference rs727504121(A;A)
Significance Pathogenic
Disease not provided Retinoblastoma
Variation info
Gene RB1
CLNDBN not provided Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.48947604delA
CLNSRC HGMD
CLNACC RCV000153809.2, RCV000174238.1,