rs387906710

Orientation

plus

Stabilized

plus

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

Make rs387906710(C;T)

Make rs387906710(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

56565362

Gene

UBQLN2

is a	snp
is	mentioned by
dbSNP	rs387906710
dbSNP (classic)	rs387906710
ClinGen	rs387906710
ebi	rs387906710
HLI	rs387906710
Exac	rs387906710
Gnomad	rs387906710
Varsome	rs387906710
LitVar	rs387906710
Map	rs387906710
PheGenI	rs387906710
Biobank	rs387906710
1000 genomes	rs387906710
hgdp	rs387906710
ensembl	rs387906710
geneview	rs387906710
scholar	rs387906710
google	rs387906710
pharmgkb	rs387906710
gwascentral	rs387906710
openSNP	rs387906710
23andMe	rs387906710
SNPshot	rs387906710
SNPdbe	rs387906710
MSV3d	rs387906710
GWAS Ctlg	rs387906710

Max Magnitude

0

ClinVar
Risk	rs387906710(T;T)
Alt	rs387906710(T;T)
Reference	Rs387906710(C;C)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis 15
Variation	info
Gene	UBQLN2
CLNDBN	Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia
Reversed	0
HGVS	NC_000023.10:g.56591795C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000022843.13,