rs121909331

Orientation

minus

Stabilized

minus

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

Make rs121909331(A;A)

Make rs121909331(A;C)

Reference

GRCh38 38.1/141

Chromosome

9

Position

35064167

Gene

VCP

is a	snp
is	mentioned by
dbSNP	rs121909331
dbSNP (classic)	rs121909331
ClinGen	rs121909331
ebi	rs121909331
HLI	rs121909331
Exac	rs121909331
Gnomad	rs121909331
Varsome	rs121909331
LitVar	rs121909331
Map	rs121909331
PheGenI	rs121909331
Biobank	rs121909331
1000 genomes	rs121909331
hgdp	rs121909331
ensembl	rs121909331
geneview	rs121909331
scholar	rs121909331
google	rs121909331
pharmgkb	rs121909331
gwascentral	rs121909331
openSNP	rs121909331
23andMe	rs121909331
SNPshot	rs121909331
SNPdbe	rs121909331
MSV3d	rs121909331
GWAS Ctlg	rs121909331

Max Magnitude

0

OMIM	601023
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121909331(A;A)
Alt	rs121909331(A;A)
Reference	Rs121909331(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.35064164G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008991.2,