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rs121909330

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909330(C;T)
Make rs121909330(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position35065364
GeneVCP
is asnp
is mentioned by
dbSNPrs121909330
ebirs121909330
HLIrs121909330
Exacrs121909330
Varsomers121909330
Maprs121909330
PheGenIrs121909330
hapmaprs121909330
1000 genomesrs121909330
hgdprs121909330
ensemblrs121909330
gopubmedrs121909330
geneviewrs121909330
scholarrs121909330
googlers121909330
pharmgkbrs121909330
gwascentralrs121909330
openSNPrs121909330
23andMers121909330
23andMe allrs121909330
SNP Nexus

SNPshotrs121909330
SNPdbers121909330
MSV3drs121909330
GWAS Ctlgrs121909330
Max Magnitude0
OMIM601023
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909330(T;T)
Alt rs121909330(T;T)
Reference rs121909330(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.35065361G>A; NC_000009.11:g.35065361G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008990.3, RCV000196145.1,