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rs753084727

From SNPedia

Orientationplus
Make rs753084727(-;-)
Make rs753084727(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position66565841
GeneCTSF
is asnp
is mentioned by
dbSNPrs753084727
ebirs753084727
HLIrs753084727
Exacrs753084727
Varsomers753084727
Maprs753084727
PheGenIrs753084727
hapmaprs753084727
1000 genomesrs753084727
hgdprs753084727
ensemblrs753084727
gopubmedrs753084727
geneviewrs753084727
scholarrs753084727
googlers753084727
pharmgkbrs753084727
gwascentralrs753084727
openSNPrs753084727
23andMers753084727
23andMe allrs753084727
SNP Nexus

SNPshotrs753084727
SNPdbers753084727
MSV3drs753084727
GWAS Ctlgrs753084727
Max Magnitude
ClinVar
Risk rs753084727(;)
Alt rs753084727(;)
Reference rs753084727(G;G)
Significance Pathogenic
Disease Ceroid lipofuscinosis
Variation info
Gene CTSF
CLNDBN Ceroid lipofuscinosis, neuronal, 13
Reversed 0
HGVS NC_000011.9:g.66333312delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000054494.4,