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rs397514732

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514732(C;C)
Make rs397514732(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position66564095
GeneCTSF
is asnp
is mentioned by
dbSNPrs397514732
ebirs397514732
HLIrs397514732
Exacrs397514732
Varsomers397514732
Maprs397514732
PheGenIrs397514732
hapmaprs397514732
1000 genomesrs397514732
hgdprs397514732
ensemblrs397514732
gopubmedrs397514732
geneviewrs397514732
scholarrs397514732
googlers397514732
pharmgkbrs397514732
gwascentralrs397514732
openSNPrs397514732
23andMers397514732
23andMe allrs397514732
SNP Nexus

SNPshotrs397514732
SNPdbers397514732
MSV3drs397514732
GWAS Ctlgrs397514732
Max Magnitude0
ClinVar
Risk rs397514732(C;C)
Alt rs397514732(C;C)
Reference rs397514732(G;G)
Significance Pathogenic
Disease Ceroid lipofuscinosis
Variation info
Gene CTSF
CLNDBN Ceroid lipofuscinosis, neuronal, 13
Reversed 1
HGVS NC_000011.9:g.66331566C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000054491.3,