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rs121434241

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434241(C;T)
Make rs121434241(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position150344216
GenePRPF3
is asnp
is mentioned by
dbSNPrs121434241
ebirs121434241
HLIrs121434241
Exacrs121434241
Varsomers121434241
Maprs121434241
PheGenIrs121434241
hapmaprs121434241
1000 genomesrs121434241
hgdprs121434241
ensemblrs121434241
gopubmedrs121434241
geneviewrs121434241
scholarrs121434241
googlers121434241
pharmgkbrs121434241
gwascentralrs121434241
openSNPrs121434241
23andMers121434241
23andMe allrs121434241
SNP Nexus

SNPshotrs121434241
SNPdbers121434241
MSV3drs121434241
GWAS Ctlgrs121434241
Max Magnitude0
OMIM607301
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434241(T;T)
Alt rs121434241(T;T)
Reference rs121434241(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 18
Variation info
Gene PRPF3
CLNDBN Retinitis pigmentosa 18
Reversed 0
HGVS NC_000001.10:g.150316692C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003516.2,