rs863225291

Orientation

minus

Stabilized

minus

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

Make rs863225291(A;T)

Make rs863225291(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

35067922

Gene

VCP

is a	snp
is	mentioned by
dbSNP	rs863225291
dbSNP (classic)	rs863225291
ClinGen	rs863225291
ebi	rs863225291
HLI	rs863225291
Exac	rs863225291
Gnomad	rs863225291
Varsome	rs863225291
LitVar	rs863225291
Map	rs863225291
PheGenI	rs863225291
Biobank	rs863225291
1000 genomes	rs863225291
hgdp	rs863225291
ensembl	rs863225291
geneview	rs863225291
scholar	rs863225291
google	rs863225291
pharmgkb	rs863225291
gwascentral	rs863225291
openSNP	rs863225291
23andMe	rs863225291
SNPshot	rs863225291
SNPdbe	rs863225291
MSV3d	rs863225291
GWAS Ctlg	rs863225291

Max Magnitude

0

ClinVar
Risk	rs863225291(T;T)
Alt	rs863225291(T;T)
Reference	Rs863225291(A;A)
Significance	Probable-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.35067919T>A
CLNSRC
CLNACC	RCV000201935.1,