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rs397514516

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397514516(C;C)
Make rs397514516(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position24082562
GeneNRL
is asnp
is mentioned by
dbSNPrs397514516
ebirs397514516
HLIrs397514516
Exacrs397514516
Varsomers397514516
Maprs397514516
PheGenIrs397514516
hapmaprs397514516
1000 genomesrs397514516
hgdprs397514516
ensemblrs397514516
gopubmedrs397514516
geneviewrs397514516
scholarrs397514516
googlers397514516
pharmgkbrs397514516
gwascentralrs397514516
openSNPrs397514516
23andMers397514516
23andMe allrs397514516
SNP Nexus

SNPshotrs397514516
SNPdbers397514516
MSV3drs397514516
GWAS Ctlgrs397514516
Max Magnitude0
ClinVar
Risk rs397514516(C;C)
Alt rs397514516(C;C)
Reference rs397514516(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 27
Variation info
Gene NRL
CLNDBN Retinitis pigmentosa 27
Reversed 1
HGVS NC_000014.8:g.24551771A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000032706.25,