rs864309501

Orientation

minus

Stabilized

minus

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

Make rs864309501(A;A)

Make rs864309501(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

35065274

Gene

VCP

is a	snp
is	mentioned by
dbSNP	rs864309501
dbSNP (classic)	rs864309501
ClinGen	rs864309501
ebi	rs864309501
HLI	rs864309501
Exac	rs864309501
Gnomad	rs864309501
Varsome	rs864309501
LitVar	rs864309501
Map	rs864309501
PheGenI	rs864309501
Biobank	rs864309501
1000 genomes	rs864309501
hgdp	rs864309501
ensembl	rs864309501
geneview	rs864309501
scholar	rs864309501
google	rs864309501
pharmgkb	rs864309501
gwascentral	rs864309501
openSNP	rs864309501
23andMe	rs864309501
SNPshot	rs864309501
SNPdbe	rs864309501
MSV3d	rs864309501
GWAS Ctlg	rs864309501

Max Magnitude

0

ClinVar
Risk	rs864309501(A;A)
Alt	rs864309501(A;A)
Reference	Rs864309501(G;G)
Significance	Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	VCP
CLNDBN	Charcot-Marie-Tooth disease, axonal, type 2y
Reversed	1
HGVS	NC_000009.11:g.35065271C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000202444.2,