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rs121909398

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909398(C;T)
Make rs121909398(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position181558617
GeneCERKL
is asnp
is mentioned by
dbSNPrs121909398
ebirs121909398
HLIrs121909398
Exacrs121909398
Varsomers121909398
Maprs121909398
PheGenIrs121909398
hapmaprs121909398
1000 genomesrs121909398
hgdprs121909398
ensemblrs121909398
gopubmedrs121909398
geneviewrs121909398
scholarrs121909398
googlers121909398
pharmgkbrs121909398
gwascentralrs121909398
openSNPrs121909398
23andMers121909398
23andMe allrs121909398
SNP Nexus

SNPshotrs121909398
SNPdbers121909398
MSV3drs121909398
GWAS Ctlgrs121909398
GMAF0.0004591
Max Magnitude0
OMIM608381
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909398(G,T;G,T)
Alt rs121909398(G,T;G,T)
Reference rs121909398(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 26
Variation info
Gene CERKL
CLNDBN Retinitis pigmentosa 26
Reversed 1
HGVS NC_000002.11:g.182423344G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002460.4, RCV000196604.1,