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rs587779411

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779411(C;G)
Make rs587779411(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position1780498
GeneCLN8
is asnp
is mentioned by
dbSNPrs587779411
ebirs587779411
HLIrs587779411
Exacrs587779411
Varsomers587779411
Maprs587779411
PheGenIrs587779411
hapmaprs587779411
1000 genomesrs587779411
hgdprs587779411
ensemblrs587779411
gopubmedrs587779411
geneviewrs587779411
scholarrs587779411
googlers587779411
pharmgkbrs587779411
gwascentralrs587779411
openSNPrs587779411
23andMers587779411
23andMe allrs587779411
SNP Nexus

SNPshotrs587779411
SNPdbers587779411
MSV3drs587779411
GWAS Ctlgrs587779411
Max Magnitude0
ClinVar
Risk rs587779411(G;G)
Alt rs587779411(G;G)
Reference rs587779411(C;C)
Significance Pathogenic
Disease Ceroid lipofuscinosis neuronal 8
Variation info
Gene CLN8
CLNDBN Ceroid lipofuscinosis neuronal 8
Reversed 0
HGVS NC_000008.10:g.1728664C>G
CLNSRC
CLNACC RCV000087102.1, RCV000201947.1,