Rs104894463

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894463(C;C)
Make rs104894463(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position24081471
GeneNRL
is asnp
is mentioned by
dbSNPrs104894463
Exacrs104894463
PheGenIrs104894463
nextbiors104894463
hapmaprs104894463
1000 genomesrs104894463
hgdprs104894463
ensemblrs104894463
gopubmedrs104894463
geneviewrs104894463
scholarrs104894463
googlers104894463
pharmgkbrs104894463
gwascentralrs104894463
openSNPrs104894463
23andMers104894463
23andMe allrs104894463
SNP Nexus

SNPshotrs104894463
SNPdbers104894463
MSV3drs104894463
OMIM162080
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894463(C;C)
Alt rs104894463(C;C)
Reference rs104894463(T;T)
Significance Pathogenic
Disease Retinal degeneration
Variation info
Gene NRL
CLNDBN Retinal degeneration, autosomal recessive, clumped pigment type
Reversed 1
HGVS NC_000014.8:g.24550680A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015088.24,