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rs1060503075

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(CCTC;CCTC) 0 common in clinvar
Make rs1060503075(-;-)
Make rs1060503075(-;CCTC)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position48463818
GeneRB1
is asnp
is mentioned by
dbSNPrs1060503075
dbSNP (old)rs1060503075
ClinGenrs1060503075
ebirs1060503075
HLIrs1060503075
Exacrs1060503075
Gnomadrs1060503075
Varsomers1060503075
Maprs1060503075
PheGenIrs1060503075
Biobankrs1060503075
1000 genomesrs1060503075
hgdprs1060503075
ensemblrs1060503075
gopubmedrs1060503075
geneviewrs1060503075
scholarrs1060503075
googlers1060503075
pharmgkbrs1060503075
gwascentralrs1060503075
openSNPrs1060503075
23andMers1060503075
23andMe allrs1060503075
SNPshotrs1060503075
SNPdbers1060503075
MSV3drs1060503075
GWAS Ctlgrs1060503075
Max Magnitude0
ClinVar
Risk rs1060503075(-;-)
Alt rs1060503075(-;-)
Reference Rs1060503075(CCTC;CCTC)
Significance Pathogenic
Disease Retinoblastoma
Variation info
Gene RB1
CLNDBN Retinoblastoma
Reversed 0
HGVS NC_000013.10:g.49037954_49037957delCCTC
CLNSRC
CLNACC RCV000476967.1,