rs121909333

Merged into

rs121909329

Orientation

minus

Stabilized

minus

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

Make rs121909333(C;C)

Make rs121909333(C;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

35065363

Gene

VCP

is a	snp
is	mentioned by
dbSNP	rs121909333
dbSNP (classic)	rs121909333
ClinGen	rs121909333
ebi	rs121909333
HLI	rs121909333
Exac	rs121909333
Gnomad	rs121909333
Varsome	rs121909333
LitVar	rs121909333
Map	rs121909333
PheGenI	rs121909333
Biobank	rs121909333
1000 genomes	rs121909333
hgdp	rs121909333
ensembl	rs121909333
geneview	rs121909333
scholar	rs121909333
google	rs121909333
pharmgkb	rs121909333
gwascentral	rs121909333
openSNP	rs121909333
23andMe	rs121909333
SNPshot	rs121909333
SNPdbe	rs121909333
MSV3d	rs121909333
GWAS Ctlg	rs121909333

Status

Merged into rs121909329

Max Magnitude

0

OMIM	601023
Desc
Variant	0005
Related	also

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,