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rs769156393

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs769156393(C;T)
Make rs769156393(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position54622243
GeneRP1
is asnp
is mentioned by
dbSNPrs769156393
ebirs769156393
HLIrs769156393
Exacrs769156393
Varsomers769156393
Maprs769156393
PheGenIrs769156393
hapmaprs769156393
1000 genomesrs769156393
hgdprs769156393
ensemblrs769156393
gopubmedrs769156393
geneviewrs769156393
scholarrs769156393
googlers769156393
pharmgkbrs769156393
gwascentralrs769156393
openSNPrs769156393
23andMers769156393
23andMe allrs769156393
SNP Nexus

SNPshotrs769156393
SNPdbers769156393
MSV3drs769156393
GWAS Ctlgrs769156393
Max Magnitude0
ClinVar
Risk rs769156393(T;T)
Alt rs769156393(T;T)
Reference rs769156393(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene RP1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000008.10:g.55534803C>T
CLNSRC
CLNACC RCV000225575.1,