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rs794727281

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727281(C;T)
Make rs794727281(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position24082698
GeneNRL
is asnp
is mentioned by
dbSNPrs794727281
ebirs794727281
HLIrs794727281
Exacrs794727281
Varsomers794727281
Maprs794727281
PheGenIrs794727281
hapmaprs794727281
1000 genomesrs794727281
hgdprs794727281
ensemblrs794727281
gopubmedrs794727281
geneviewrs794727281
scholarrs794727281
googlers794727281
pharmgkbrs794727281
gwascentralrs794727281
openSNPrs794727281
23andMers794727281
23andMe allrs794727281
SNP Nexus

SNPshotrs794727281
SNPdbers794727281
MSV3drs794727281
GWAS Ctlgrs794727281
Max Magnitude0
ClinVar
Risk rs794727281(T;T)
Alt rs794727281(T;T)
Reference rs794727281(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 27
Variation info
Gene NRL
CLNDBN Retinitis pigmentosa 27
Reversed 1
HGVS NC_000014.8:g.24551907G>A
CLNSRC
CLNACC RCV000175819.1,