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rs869312809

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312809(G;G)
Make rs869312809(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position61915631
GeneVPS13C
is asnp
is mentioned by
dbSNPrs869312809
dbSNP (old)rs869312809
ClinGenrs869312809
ebirs869312809
HLIrs869312809
Exacrs869312809
Gnomadrs869312809
Varsomers869312809
Maprs869312809
PheGenIrs869312809
Biobankrs869312809
1000 genomesrs869312809
hgdprs869312809
ensemblrs869312809
gopubmedrs869312809
geneviewrs869312809
scholarrs869312809
googlers869312809
pharmgkbrs869312809
gwascentralrs869312809
openSNPrs869312809
23andMers869312809
23andMe allrs869312809
SNP Nexus

SNPshotrs869312809
SNPdbers869312809
MSV3drs869312809
GWAS Ctlgrs869312809
Max Magnitude0
ClinVar
Risk rs869312809(G;G)
Alt rs869312809(G;G)
Reference Rs869312809(T;T)
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.62207830A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000210216.1, RCV000236364.1,