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rs387907268

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907268(C;T)
Make rs387907268(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position76540205
GenePRCD
is asnp
is mentioned by
dbSNPrs387907268
ebirs387907268
HLIrs387907268
Exacrs387907268
Varsomers387907268
Maprs387907268
PheGenIrs387907268
hapmaprs387907268
1000 genomesrs387907268
hgdprs387907268
ensemblrs387907268
gopubmedrs387907268
geneviewrs387907268
scholarrs387907268
googlers387907268
pharmgkbrs387907268
gwascentralrs387907268
openSNPrs387907268
23andMers387907268
23andMe allrs387907268
SNP Nexus

SNPshotrs387907268
SNPdbers387907268
MSV3drs387907268
GWAS Ctlgrs387907268
Max Magnitude0
ClinVar
Risk rs387907268(T;T)
Alt rs387907268(T;T)
Reference rs387907268(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 36
Variation info
Gene PRCD
CLNDBN Retinitis pigmentosa 36
Reversed 0
HGVS NC_000017.10:g.74536287C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030701.2,