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rs369100678

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369100678(C;G)
Make rs369100678(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position61958608
GeneVPS13C
is asnp
is mentioned by
dbSNPrs369100678
ebirs369100678
HLIrs369100678
Exacrs369100678
Varsomers369100678
Maprs369100678
PheGenIrs369100678
hapmaprs369100678
1000 genomesrs369100678
hgdprs369100678
ensemblrs369100678
gopubmedrs369100678
geneviewrs369100678
scholarrs369100678
googlers369100678
pharmgkbrs369100678
gwascentralrs369100678
openSNPrs369100678
23andMers369100678
23andMe allrs369100678
SNP Nexus

SNPshotrs369100678
SNPdbers369100678
MSV3drs369100678
GWAS Ctlgrs369100678
Max Magnitude0
ClinVar
Risk rs369100678(G;G)
Alt rs369100678(G;G)
Reference rs369100678(C;C)
Significance Pathogenic
Disease Parkinson disease 23 Parkinson disease
Variation info
Gene VPS13C
CLNDBN Parkinson disease 23, autosomal recessive early-onset Parkinson disease
Reversed 0
HGVS NC_000015.9:g.62250807C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000210217.1, RCV000236463.1,