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rs772592456

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs772592456(A;A)
Make rs772592456(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position49549573
GeneRCBTB1
is asnp
is mentioned by
dbSNPrs772592456
ebirs772592456
HLIrs772592456
Exacrs772592456
Varsomers772592456
Maprs772592456
PheGenIrs772592456
hapmaprs772592456
1000 genomesrs772592456
hgdprs772592456
ensemblrs772592456
gopubmedrs772592456
geneviewrs772592456
scholarrs772592456
googlers772592456
pharmgkbrs772592456
gwascentralrs772592456
openSNPrs772592456
23andMers772592456
23andMe allrs772592456
SNP Nexus

SNPshotrs772592456
SNPdbers772592456
MSV3drs772592456
GWAS Ctlgrs772592456
Max Magnitude0
ClinVar
Risk rs772592456(A;A)
Alt rs772592456(A;A)
Reference rs772592456(C;C)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RCBTB1
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000013.10:g.50123709C>A
CLNSRC
CLNACC RCV000239602.1,