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rs869312810

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312810(G;T)
Make rs869312810(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position61882652
GeneVPS13C
is asnp
is mentioned by
dbSNPrs869312810
ebirs869312810
HLIrs869312810
Exacrs869312810
Varsomers869312810
Maprs869312810
PheGenIrs869312810
hapmaprs869312810
1000 genomesrs869312810
hgdprs869312810
ensemblrs869312810
gopubmedrs869312810
geneviewrs869312810
scholarrs869312810
googlers869312810
pharmgkbrs869312810
gwascentralrs869312810
openSNPrs869312810
23andMers869312810
23andMe allrs869312810
SNP Nexus

SNPshotrs869312810
SNPdbers869312810
MSV3drs869312810
GWAS Ctlgrs869312810
Max Magnitude0
ClinVar
Risk rs869312810(T;T)
Alt rs869312810(T;T)
Reference rs869312810(G;G)
Significance Pathogenic
Disease Parkinson disease 23 Parkinson disease
Variation info
Gene VPS13C
CLNDBN Parkinson disease 23, autosomal recessive early-onset Parkinson disease
Reversed 1
HGVS NC_000015.9:g.62174851C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210213.1, RCV000235875.1,