rs886041317

Orientation

plus

Stabilized

plus

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

Chromosome

3

Position

193642763

Gene

OPA1

is a	snp
is	mentioned by
dbSNP	rs886041317
dbSNP (classic)	rs886041317
ClinGen	rs886041317
ebi	rs886041317
HLI	rs886041317
Exac	rs886041317
Gnomad	rs886041317
Varsome	rs886041317
LitVar	rs886041317
Map	rs886041317
PheGenI	rs886041317
Biobank	rs886041317
1000 genomes	rs886041317
hgdp	rs886041317
ensembl	rs886041317
geneview	rs886041317
scholar	rs886041317
google	rs886041317
pharmgkb	rs886041317
gwascentral	rs886041317
openSNP	rs886041317
23andMe	rs886041317
SNPshot	rs886041317
SNPdbe	rs886041317
MSV3d	rs886041317
GWAS Ctlg	rs886041317

Max Magnitude

0

ClinVar
Risk	rs886041317(G;G)
Alt	rs886041317(G;G)
Reference	Rs886041317(A;A)
Significance	Pathogenic
Disease	Autosomal dominant optic atrophy plus syndrome not provided Dominant hereditary optic atrophy
Variation	info
Gene	OPA1
CLNDBN	Autosomal dominant optic atrophy plus syndrome not provided Dominant hereditary optic atrophy
Reversed	0
HGVS	NC_000003.11:g.193360552A>G
CLNSRC
CLNACC	RCV000313660.1, RCV000368869.1, RCV000398369.1,