rs121909334

Orientation

minus

Stabilized

minus

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

Make rs121909334(A;A)

Make rs121909334(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

35065255

Gene

VCP

is a	snp
is	mentioned by
dbSNP	rs121909334
dbSNP (classic)	rs121909334
ClinGen	rs121909334
ebi	rs121909334
HLI	rs121909334
Exac	rs121909334
Gnomad	rs121909334
Varsome	rs121909334
LitVar	rs121909334
Map	rs121909334
PheGenI	rs121909334
Biobank	rs121909334
1000 genomes	rs121909334
hgdp	rs121909334
ensembl	rs121909334
geneview	rs121909334
scholar	rs121909334
google	rs121909334
pharmgkb	rs121909334
gwascentral	rs121909334
openSNP	rs121909334
23andMe	rs121909334
SNPshot	rs121909334
SNPdbe	rs121909334
MSV3d	rs121909334
GWAS Ctlg	rs121909334

Max Magnitude

0

OMIM	601023
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121909334(A;A)
Alt	rs121909334(A;A)
Reference	Rs121909334(G;G)
Significance	Pathogenic
Disease	Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Amyotrophic lateral sclerosis 14
Variation	info
Gene	VCP
CLNDBN	Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia
Reversed	1
HGVS	NC_000009.11:g.35065252C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008994.3, RCV000023064.3,