rs397515506

Orientation

plus

Stabilized

plus

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

Make rs397515506(C;T)

Make rs397515506(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

14568

Gene

ND6

is a	snp
is	mentioned by
dbSNP	rs397515506
dbSNP (classic)	rs397515506
ClinGen	rs397515506
ebi	rs397515506
HLI	rs397515506
Exac	rs397515506
Gnomad	rs397515506
Varsome	rs397515506
LitVar	rs397515506
Map	rs397515506
PheGenI	rs397515506
Biobank	rs397515506
1000 genomes	rs397515506
hgdp	rs397515506
ensembl	rs397515506
geneview	rs397515506
scholar	rs397515506
google	rs397515506
pharmgkb	rs397515506
gwascentral	rs397515506
openSNP	rs397515506
23andMe	rs397515506
SNPshot	rs397515506
SNPdbe	rs397515506
MSV3d	rs397515506
GWAS Ctlg	rs397515506

Max Magnitude

0

ClinVar
Risk	rs397515506(T;T)
Alt	rs397515506(T;T)
Reference	Rs397515506(C;C)
Significance	Pathogenic
Disease	Leber's optic atrophy
Variation	info
Gene	ND6
CLNDBN	Leber's optic atrophy
Reversed	0
HGVS	NC_012920.1:m.14568C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000055703.1,