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rs121909333

From SNPedia

Merged intors121909329
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909333(C;C)
Make rs121909333(C;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position35065363
GeneVCP
is asnp
is mentioned by
dbSNPrs121909333
ebirs121909333
HLIrs121909333
Exacrs121909333
Varsomers121909333
Maprs121909333
PheGenIrs121909333
hapmaprs121909333
1000 genomesrs121909333
hgdprs121909333
ensemblrs121909333
gopubmedrs121909333
geneviewrs121909333
scholarrs121909333
googlers121909333
pharmgkbrs121909333
gwascentralrs121909333
openSNPrs121909333
23andMers121909333
23andMe allrs121909333
SNP Nexus

SNPshotrs121909333
SNPdbers121909333
MSV3drs121909333
GWAS Ctlgrs121909333
StatusMerged into rs121909329
Max Magnitude0
OMIM601023
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909333(C;C)
Alt rs121909333(C;C)
Reference rs121909333(G;G)
Significance Pathogenic
Disease Inclusion body myopathy with early-onset paget disease and front
Variation info
Gene VCP
CLNDBN Inclusion body myopathy with early-onset paget disease and front
Reversed 1
HGVS NC_000009.11:g.35065360C>G
CLNSRC OMIM Allelic Variant
CLNACC SCV000029207.1,