rs387906790

Orientation

minus

Stabilized

minus

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

Make rs387906790(A;A)

Make rs387906790(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

35059723

Gene

VCP

is a	snp
is	mentioned by
dbSNP	rs387906790
dbSNP (classic)	rs387906790
ClinGen	rs387906790
ebi	rs387906790
HLI	rs387906790
Exac	rs387906790
Gnomad	rs387906790
Varsome	rs387906790
LitVar	rs387906790
Map	rs387906790
PheGenI	rs387906790
Biobank	rs387906790
1000 genomes	rs387906790
hgdp	rs387906790
ensembl	rs387906790
geneview	rs387906790
scholar	rs387906790
google	rs387906790
pharmgkb	rs387906790
gwascentral	rs387906790
openSNP	rs387906790
23andMe	rs387906790
SNPshot	rs387906790
SNPdbe	rs387906790
MSV3d	rs387906790
GWAS Ctlg	rs387906790

Max Magnitude

0

ClinVar
Risk	rs387906790(A;A)
Alt	rs387906790(A;A)
Reference	Rs387906790(G;G)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis 14 without frontotemporal dementia
Variation	info
Gene	VCP
CLNDBN	Amyotrophic lateral sclerosis 14 without frontotemporal dementia
Reversed	1
HGVS	NC_000009.11:g.35059720C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023066.2,