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rs863225291

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225291(A;T)
Make rs863225291(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position35067922
GeneVCP
is asnp
is mentioned by
dbSNPrs863225291
ebirs863225291
HLIrs863225291
Exacrs863225291
Varsomers863225291
Maprs863225291
PheGenIrs863225291
hapmaprs863225291
1000 genomesrs863225291
hgdprs863225291
ensemblrs863225291
gopubmedrs863225291
geneviewrs863225291
scholarrs863225291
googlers863225291
pharmgkbrs863225291
gwascentralrs863225291
openSNPrs863225291
23andMers863225291
23andMe allrs863225291
SNP Nexus

SNPshotrs863225291
SNPdbers863225291
MSV3drs863225291
GWAS Ctlgrs863225291
Max Magnitude0
ClinVar
Risk rs863225291(T;T)
Alt rs863225291(T;T)
Reference rs863225291(A;A)
Significance Probable-Pathogenic
Disease Inclusion body myopathy with early-onset paget disease and frontotemporal dementia
Variation info
Gene VCP
CLNDBN Inclusion body myopathy with early-onset paget disease and frontotemporal dementia
Reversed 1
HGVS NC_000009.11:g.35067919T>A
CLNSRC
CLNACC RCV000201935.1,