Rs104894459

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894459(A;A)
Make rs104894459(A;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position24082701
GeneNRL
is asnp
is mentioned by
dbSNPrs104894459
Exacrs104894459
PheGenIrs104894459
nextbiors104894459
hapmaprs104894459
1000 genomesrs104894459
hgdprs104894459
ensemblrs104894459
gopubmedrs104894459
geneviewrs104894459
scholarrs104894459
googlers104894459
pharmgkbrs104894459
gwascentralrs104894459
openSNPrs104894459
23andMers104894459
23andMe allrs104894459
SNP Nexus

SNPshotrs104894459
SNPdbers104894459
MSV3drs104894459
Max Magnitude0
OMIM162080
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894459(A;A)
Alt rs104894459(A;A)
Reference rs104894459(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 27
Variation info
Gene NRL
CLNDBN Retinitis pigmentosa 27
Reversed 1
HGVS NC_000014.8:g.24551910A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015086.20,