Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779409

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779409(C;T)
Make rs587779409(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position1758970
GeneCTSD
is asnp
is mentioned by
dbSNPrs587779409
ebirs587779409
HLIrs587779409
Exacrs587779409
Varsomers587779409
Maprs587779409
PheGenIrs587779409
hapmaprs587779409
1000 genomesrs587779409
hgdprs587779409
ensemblrs587779409
gopubmedrs587779409
geneviewrs587779409
scholarrs587779409
googlers587779409
pharmgkbrs587779409
gwascentralrs587779409
openSNPrs587779409
23andMers587779409
23andMe allrs587779409
SNP Nexus

SNPshotrs587779409
SNPdbers587779409
MSV3drs587779409
GWAS Ctlgrs587779409
Max Magnitude0
ClinVar
Risk rs587779409(T;T)
Alt rs587779409(T;T)
Reference rs587779409(C;C)
Significance Pathogenic
Disease Ceroid lipofuscinosis neuronal 10
Variation info
Gene CTSD
CLNDBN Ceroid lipofuscinosis neuronal 10
Reversed 1
HGVS NC_000011.9:g.1780200G>A
CLNSRC
CLNACC RCV000087098.1,