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rs527236087

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs527236087(-;-)
Make rs527236087(-;T)
ReferenceGRCh38 38.1/142
Chromosome14
Position24082826
GeneNRL
is asnp
is mentioned by
dbSNPrs527236087
ebirs527236087
HLIrs527236087
Exacrs527236087
Varsomers527236087
Maprs527236087
PheGenIrs527236087
hapmaprs527236087
1000 genomesrs527236087
hgdprs527236087
ensemblrs527236087
gopubmedrs527236087
geneviewrs527236087
scholarrs527236087
googlers527236087
pharmgkbrs527236087
gwascentralrs527236087
openSNPrs527236087
23andMers527236087
23andMe allrs527236087
SNP Nexus

SNPshotrs527236087
SNPdbers527236087
MSV3drs527236087
GWAS Ctlgrs527236087
Max Magnitude0
ClinVar
Risk rs527236087(;)
Alt rs527236087(;)
Reference rs527236087(T;T)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene NRL
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000014.8:g.24552035delA
CLNSRC ClinVar
CLNACC RCV000132657.1,