rs895824243

Orientation

plus

Stabilized

plus

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

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

13110387

Gene

OPTN

is a	snp
is	mentioned by
dbSNP	rs895824243
dbSNP (classic)	rs895824243
ClinGen	rs895824243
ebi	rs895824243
HLI	rs895824243
Exac	rs895824243
Gnomad	rs895824243
Varsome	rs895824243
LitVar	rs895824243
Map	rs895824243
PheGenI	rs895824243
Biobank	rs895824243
1000 genomes	rs895824243
hgdp	rs895824243
ensembl	rs895824243
geneview	rs895824243
scholar	rs895824243
google	rs895824243
pharmgkb	rs895824243
gwascentral	rs895824243
openSNP	rs895824243
23andMe	rs895824243
SNPshot	rs895824243
SNPdbe	rs895824243
MSV3d	rs895824243
GWAS Ctlg	rs895824243

Max Magnitude

0

ClinVar
Risk	rs895824243(C;C)
Alt	rs895824243(C;C)
Reference	Rs895824243(A;A)
Significance	Probable-Pathogenic
Disease	Motor neuron disease
Variation	info
Gene
CLNDBN	Motor neuron disease
Reversed	0
HGVS	NC_000010.10:g.13152387A>C
CLNSRC
CLNACC	RCV000492199.1,