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rs398122964

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398122964(-;-)
Make rs398122964(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position181558606
GeneCERKL
is asnp
is mentioned by
dbSNPrs398122964
ebirs398122964
HLIrs398122964
Exacrs398122964
Varsomers398122964
Maprs398122964
PheGenIrs398122964
hapmaprs398122964
1000 genomesrs398122964
hgdprs398122964
ensemblrs398122964
gopubmedrs398122964
geneviewrs398122964
scholarrs398122964
googlers398122964
pharmgkbrs398122964
gwascentralrs398122964
openSNPrs398122964
23andMers398122964
23andMe allrs398122964
SNP Nexus

SNPshotrs398122964
SNPdbers398122964
MSV3drs398122964
GWAS Ctlgrs398122964
Max Magnitude0
ClinVar
Risk rs398122964(;)
Alt rs398122964(;)
Reference rs398122964(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 26
Variation info
Gene CERKL
CLNDBN Retinitis pigmentosa 26
Reversed 1
HGVS NC_000002.11:g.182423333delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000076912.4,