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rs121909329

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909329(A;A)
Make rs121909329(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position35065363
GeneVCP
is asnp
is mentioned by
dbSNPrs121909329
ebirs121909329
HLIrs121909329
Exacrs121909329
Varsomers121909329
Maprs121909329
PheGenIrs121909329
hapmaprs121909329
1000 genomesrs121909329
hgdprs121909329
ensemblrs121909329
gopubmedrs121909329
geneviewrs121909329
scholarrs121909329
googlers121909329
pharmgkbrs121909329
gwascentralrs121909329
openSNPrs121909329
23andMers121909329
23andMe allrs121909329
SNP Nexus

SNPshotrs121909329
SNPdbers121909329
MSV3drs121909329
GWAS Ctlgrs121909329
Merged fromRs121909333
Max Magnitude0
OMIM601023
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909329(A,C;A,C)
Alt rs121909329(A,C;A,C)
Reference rs121909329(G;G)
Significance Pathogenic
Disease Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Amyotrophic lateral sclerosis 14 without frontotemporal dementia
Variation info
Gene VCP
CLNDBN Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Amyotrophic lateral sclerosis 14 without frontotemporal dementia
Reversed 1
HGVS NC_000009.11:g.35065360C>G; NC_000009.11:g.35065360C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008993.3, RCV000008989.2, RCV000023063.2,