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rs863224859

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224859(C;T)
Make rs863224859(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position1771266
GeneCLN8
is asnp
is mentioned by
dbSNPrs863224859
ebirs863224859
HLIrs863224859
Exacrs863224859
Varsomers863224859
Maprs863224859
PheGenIrs863224859
hapmaprs863224859
1000 genomesrs863224859
hgdprs863224859
ensemblrs863224859
gopubmedrs863224859
geneviewrs863224859
scholarrs863224859
googlers863224859
pharmgkbrs863224859
gwascentralrs863224859
openSNPrs863224859
23andMers863224859
23andMe allrs863224859
SNP Nexus

SNPshotrs863224859
SNPdbers863224859
MSV3drs863224859
GWAS Ctlgrs863224859
Max Magnitude0
ClinVar
Risk rs863224859(T;T)
Alt rs863224859(T;T)
Reference rs863224859(C;C)
Significance Probable-Pathogenic
Disease Ceroid lipofuscinosis neuronal 8
Variation info
Gene CLN8
CLNDBN Ceroid lipofuscinosis neuronal 8
Reversed 0
HGVS NC_000008.10:g.1719432C>T
CLNSRC
CLNACC RCV000197221.1,