rs786205611

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(I;I)	0	common genotype
(TGACA;TGACA)	0	common in clinvar

Make rs786205611(-;-)

Make rs786205611(-;TGACA)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

13124029

Gene

OPTN

is a	snp
is	mentioned by
dbSNP	rs786205611
dbSNP (classic)	rs786205611
ClinGen	rs786205611
ebi	rs786205611
HLI	rs786205611
Exac	rs786205611
Gnomad	rs786205611
Varsome	rs786205611
LitVar	rs786205611
Map	rs786205611
PheGenI	rs786205611
Biobank	rs786205611
1000 genomes	rs786205611
hgdp	rs786205611
ensembl	rs786205611
geneview	rs786205611
scholar	rs786205611
google	rs786205611
pharmgkb	rs786205611
gwascentral	rs786205611
openSNP	rs786205611
23andMe	rs786205611
SNPshot	rs786205611
SNPdbe	rs786205611
MSV3d	rs786205611
GWAS Ctlg	rs786205611

Max Magnitude

0

ClinVar
Risk	rs786205611(-;-)
Alt	rs786205611(-;-)
Reference	Rs786205611(TGACA;TGACA)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	OPTN
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.13166029_13166033delTGACA
CLNSRC
CLNACC	RCV000171456.1,