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rs121909335

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909335(A;A)
Make rs121909335(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position35065351
GeneVCP
is asnp
is mentioned by
dbSNPrs121909335
ebirs121909335
HLIrs121909335
Exacrs121909335
Varsomers121909335
Maprs121909335
PheGenIrs121909335
hapmaprs121909335
1000 genomesrs121909335
hgdprs121909335
ensemblrs121909335
gopubmedrs121909335
geneviewrs121909335
scholarrs121909335
googlers121909335
pharmgkbrs121909335
gwascentralrs121909335
openSNPrs121909335
23andMers121909335
23andMe allrs121909335
SNP Nexus

SNPshotrs121909335
SNPdbers121909335
MSV3drs121909335
GWAS Ctlgrs121909335
Max Magnitude0
OMIM601023
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121909335(A;A)
Alt rs121909335(A;A)
Reference rs121909335(G;G)
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.35065348C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008995.2,