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rs797045136

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045136(C;C)
Make rs797045136(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position66568273
GeneCTSF
is asnp
is mentioned by
dbSNPrs797045136
ebirs797045136
HLIrs797045136
Exacrs797045136
Varsomers797045136
Maprs797045136
PheGenIrs797045136
hapmaprs797045136
1000 genomesrs797045136
hgdprs797045136
ensemblrs797045136
gopubmedrs797045136
geneviewrs797045136
scholarrs797045136
googlers797045136
pharmgkbrs797045136
gwascentralrs797045136
openSNPrs797045136
23andMers797045136
23andMe allrs797045136
SNP Nexus

SNPshotrs797045136
SNPdbers797045136
MSV3drs797045136
GWAS Ctlgrs797045136
Max Magnitude0
ClinVar
Risk rs797045136(C;C)
Alt rs797045136(C;C)
Reference rs797045136(G;G)
Significance Pathogenic
Disease Ceroid lipofuscinosis
Variation info
Gene CTSF
CLNDBN Ceroid lipofuscinosis, neuronal, 13
Reversed 1
HGVS NC_000011.9:g.66335744C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000190878.2,