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rs121909334

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909334(A;A)
Make rs121909334(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position35065255
GeneVCP
is asnp
is mentioned by
dbSNPrs121909334
ebirs121909334
HLIrs121909334
Exacrs121909334
Varsomers121909334
Maprs121909334
PheGenIrs121909334
hapmaprs121909334
1000 genomesrs121909334
hgdprs121909334
ensemblrs121909334
gopubmedrs121909334
geneviewrs121909334
scholarrs121909334
googlers121909334
pharmgkbrs121909334
gwascentralrs121909334
openSNPrs121909334
23andMers121909334
23andMe allrs121909334
SNP Nexus

SNPshotrs121909334
SNPdbers121909334
MSV3drs121909334
GWAS Ctlgrs121909334
Max Magnitude0
OMIM601023
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909334(A;A)
Alt rs121909334(A;A)
Reference rs121909334(G;G)
Significance Pathogenic
Disease Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Amyotrophic lateral sclerosis 14
Variation info
Gene VCP
CLNDBN Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia
Reversed 1
HGVS NC_000009.11:g.35065252C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008994.2, RCV000023064.2,