Have questions? Visit https://www.reddit.com/r/SNPedia

rs879255547

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255547(G;T)
Make rs879255547(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position49544745
GeneRCBTB1
is asnp
is mentioned by
dbSNPrs879255547
ebirs879255547
HLIrs879255547
Exacrs879255547
Varsomers879255547
Maprs879255547
PheGenIrs879255547
hapmaprs879255547
1000 genomesrs879255547
hgdprs879255547
ensemblrs879255547
gopubmedrs879255547
geneviewrs879255547
scholarrs879255547
googlers879255547
pharmgkbrs879255547
gwascentralrs879255547
openSNPrs879255547
23andMers879255547
23andMe allrs879255547
SNP Nexus

SNPshotrs879255547
SNPdbers879255547
MSV3drs879255547
GWAS Ctlgrs879255547
Max Magnitude0
ClinVar
Risk rs879255547(T;T)
Alt rs879255547(T;T)
Reference rs879255547(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RCBTB1
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000013.10:g.50118881C>A
CLNSRC
CLNACC RCV000239603.1,