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rs121918561

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCT;GCT) 0 common in clinvar
Make rs121918561(-;-)
Make rs121918561(-;TGC)
Make rs121918561(TGC;TGC)
ReferenceGRCh38 38.1/141
Chromosome6
Position42721981
GenePRPH2
is asnp
is mentioned by
dbSNPrs121918561
ebirs121918561
HLIrs121918561
Exacrs121918561
Varsomers121918561
Maprs121918561
PheGenIrs121918561
hapmaprs121918561
1000 genomesrs121918561
hgdprs121918561
ensemblrs121918561
gopubmedrs121918561
geneviewrs121918561
scholarrs121918561
googlers121918561
pharmgkbrs121918561
gwascentralrs121918561
openSNPrs121918561
23andMers121918561
23andMe allrs121918561
SNP Nexus

SNPshotrs121918561
SNPdbers121918561
MSV3drs121918561
GWAS Ctlgrs121918561
Max Magnitude0
OMIM179605
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918561(;)
Alt rs121918561(;)
Reference rs121918561(GCT;GCT)
Significance Pathogenic
Disease Retinitis pigmentosa 7 not provided
Variation info
Gene PRPH2
CLNDBN Retinitis pigmentosa 7 not provided
Reversed 1
HGVS NC_000006.11:g.42689715_42689717delAGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000014048.24, RCV000084963.1,