rs397515507

Orientation

plus

Stabilized

plus

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

Make rs397515507(A;A)

Make rs397515507(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

3635

Gene

ND1

is a	snp
is	mentioned by
dbSNP	rs397515507
dbSNP (classic)	rs397515507
ClinGen	rs397515507
ebi	rs397515507
HLI	rs397515507
Exac	rs397515507
Gnomad	rs397515507
Varsome	rs397515507
LitVar	rs397515507
Map	rs397515507
PheGenI	rs397515507
Biobank	rs397515507
1000 genomes	rs397515507
hgdp	rs397515507
ensembl	rs397515507
geneview	rs397515507
scholar	rs397515507
google	rs397515507
pharmgkb	rs397515507
gwascentral	rs397515507
openSNP	rs397515507
23andMe	rs397515507
SNPshot	rs397515507
SNPdbe	rs397515507
MSV3d	rs397515507
GWAS Ctlg	rs397515507

Max Magnitude

0

ClinVar
Risk	rs397515507(A;A)
Alt	rs397515507(A;A)
Reference	Rs397515507(G;G)
Significance	Pathogenic
Disease	Leber's optic atrophy
Variation	info
Gene	ND1
CLNDBN	Leber's optic atrophy
Reversed	0
HGVS	NC_012920.1:m.3635G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000055707.1,