rs121909335

Orientation

minus

Stabilized

minus

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

Make rs121909335(A;A)

Make rs121909335(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

35065351

Gene

VCP

is a	snp
is	mentioned by
dbSNP	rs121909335
dbSNP (classic)	rs121909335
ClinGen	rs121909335
ebi	rs121909335
HLI	rs121909335
Exac	rs121909335
Gnomad	rs121909335
Varsome	rs121909335
LitVar	rs121909335
Map	rs121909335
PheGenI	rs121909335
Biobank	rs121909335
1000 genomes	rs121909335
hgdp	rs121909335
ensembl	rs121909335
geneview	rs121909335
scholar	rs121909335
google	rs121909335
pharmgkb	rs121909335
gwascentral	rs121909335
openSNP	rs121909335
23andMe	rs121909335
SNPshot	rs121909335
SNPdbe	rs121909335
MSV3d	rs121909335
GWAS Ctlg	rs121909335

Max Magnitude

0

OMIM	601023
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121909335(A;A)
Alt	rs121909335(A;A)
Reference	Rs121909335(G;G)
Significance	Pathogenic
Disease	Inclusion body myopathy with early-onset paget disease and frontotemporal dementia not provided
Variation	info
Gene	VCP
CLNDBN	Inclusion body myopathy with early-onset paget disease and frontotemporal dementia not provided
Reversed	1
HGVS	NC_000009.11:g.35065348C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008995.3, RCV000276565.1,