rs397515509

Orientation

plus

Stabilized

plus

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

Make rs397515509(C;T)

Make rs397515509(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

4025

Gene

ND1

is a	snp
is	mentioned by
dbSNP	rs397515509
dbSNP (classic)	rs397515509
ClinGen	rs397515509
ebi	rs397515509
HLI	rs397515509
Exac	rs397515509
Gnomad	rs397515509
Varsome	rs397515509
LitVar	rs397515509
Map	rs397515509
PheGenI	rs397515509
Biobank	rs397515509
1000 genomes	rs397515509
hgdp	rs397515509
ensembl	rs397515509
geneview	rs397515509
scholar	rs397515509
google	rs397515509
pharmgkb	rs397515509
gwascentral	rs397515509
openSNP	rs397515509
23andMe	rs397515509
SNPshot	rs397515509
SNPdbe	rs397515509
MSV3d	rs397515509
GWAS Ctlg	rs397515509

Max Magnitude

0

ClinVar
Risk	rs397515509(A;A) rs397515509(G;G) rs397515509(T;T)
Alt	rs397515509(A;A) rs397515509(G;G) rs397515509(T;T)
Reference	Rs397515509(C;C)
Significance	Pathogenic
Disease	Leber's optic atrophy
Variation	info
Gene	ND1
CLNDBN	Leber's optic atrophy
Reversed	0
HGVS	NC_012920.1:m.4025C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000055709.1,