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rs121918369

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918369(A;A)
Make rs121918369(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position76540146
GenePRCD
is asnp
is mentioned by
dbSNPrs121918369
ebirs121918369
HLIrs121918369
Exacrs121918369
Varsomers121918369
Maprs121918369
PheGenIrs121918369
hapmaprs121918369
1000 genomesrs121918369
hgdprs121918369
ensemblrs121918369
gopubmedrs121918369
geneviewrs121918369
scholarrs121918369
googlers121918369
pharmgkbrs121918369
gwascentralrs121918369
openSNPrs121918369
23andMers121918369
23andMe allrs121918369
SNP Nexus

SNPshotrs121918369
SNPdbers121918369
MSV3drs121918369
GWAS Ctlgrs121918369
Max Magnitude0
OMIM610598
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918369(A;A)
Alt rs121918369(A;A)
Reference rs121918369(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 36
Variation info
Gene PRCD
CLNDBN Retinitis pigmentosa 36
Reversed 0
HGVS NC_000017.10:g.74536228G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001247.2,