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rs121909332

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909332(C;G)
Make rs121909332(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position35067910
GeneVCP
is asnp
is mentioned by
dbSNPrs121909332
ebirs121909332
HLIrs121909332
Exacrs121909332
Varsomers121909332
Maprs121909332
PheGenIrs121909332
hapmaprs121909332
1000 genomesrs121909332
hgdprs121909332
ensemblrs121909332
gopubmedrs121909332
geneviewrs121909332
scholarrs121909332
googlers121909332
pharmgkbrs121909332
gwascentralrs121909332
openSNPrs121909332
23andMers121909332
23andMe allrs121909332
SNP Nexus

SNPshotrs121909332
SNPdbers121909332
MSV3drs121909332
GWAS Ctlgrs121909332
Max Magnitude0
OMIM601023
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909332(G,T;G,T)
Alt rs121909332(G,T;G,T)
Reference rs121909332(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.35067907G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008992.2,