rs121909332

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121909332(C;G)

Make rs121909332(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

35067910

Gene

VCP

is a	snp
is	mentioned by
dbSNP	rs121909332
dbSNP (classic)	rs121909332
ClinGen	rs121909332
ebi	rs121909332
HLI	rs121909332
Exac	rs121909332
Gnomad	rs121909332
Varsome	rs121909332
LitVar	rs121909332
Map	rs121909332
PheGenI	rs121909332
Biobank	rs121909332
1000 genomes	rs121909332
hgdp	rs121909332
ensembl	rs121909332
geneview	rs121909332
scholar	rs121909332
google	rs121909332
pharmgkb	rs121909332
gwascentral	rs121909332
openSNP	rs121909332
23andMe	rs121909332
SNPshot	rs121909332
SNPdbe	rs121909332
MSV3d	rs121909332
GWAS Ctlg	rs121909332

Max Magnitude

0

OMIM	601023
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121909332(G;G) rs121909332(T;T)
Alt	rs121909332(G;G) rs121909332(T;T)
Reference	Rs121909332(C;C)
Significance	Pathogenic
Disease	not provided Inclusion body myopathy with early-onset paget disease and frontotemporal dementia
Variation	info
Gene	VCP
CLNDBN	not provided Inclusion body myopathy with early-onset paget disease and frontotemporal dementia
Reversed	1
HGVS	NC_000009.11:g.35067907G>A; NC_000009.11:g.35067907G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000280148.1, RCV000008992.3,