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rs121909331

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909331(A;A)
Make rs121909331(A;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position35064167
GeneVCP
is asnp
is mentioned by
dbSNPrs121909331
ebirs121909331
HLIrs121909331
Exacrs121909331
Varsomers121909331
Maprs121909331
PheGenIrs121909331
hapmaprs121909331
1000 genomesrs121909331
hgdprs121909331
ensemblrs121909331
gopubmedrs121909331
geneviewrs121909331
scholarrs121909331
googlers121909331
pharmgkbrs121909331
gwascentralrs121909331
openSNPrs121909331
23andMers121909331
23andMe allrs121909331
SNP Nexus

SNPshotrs121909331
SNPdbers121909331
MSV3drs121909331
GWAS Ctlgrs121909331
Max Magnitude0
OMIM601023
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909331(A;A)
Alt rs121909331(A;A)
Reference rs121909331(C;C)
Significance 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.35064164G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008991.2,