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rs368217569

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368217569(C;T)
Make rs368217569(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position49549584
GeneRCBTB1
is asnp
is mentioned by
dbSNPrs368217569
ebirs368217569
HLIrs368217569
Exacrs368217569
Varsomers368217569
Maprs368217569
PheGenIrs368217569
hapmaprs368217569
1000 genomesrs368217569
hgdprs368217569
ensemblrs368217569
gopubmedrs368217569
geneviewrs368217569
scholarrs368217569
googlers368217569
pharmgkbrs368217569
gwascentralrs368217569
openSNPrs368217569
23andMers368217569
23andMe allrs368217569
SNP Nexus

SNPshotrs368217569
SNPdbers368217569
MSV3drs368217569
GWAS Ctlgrs368217569
Max Magnitude0
ClinVar
Risk rs368217569(T;T)
Alt rs368217569(T;T)
Reference rs368217569(C;C)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RCBTB1
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000013.10:g.50123720C>T
CLNSRC
CLNACC RCV000239609.1,