rs267606899

Orientation

plus

Stabilized

plus

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

Make rs267606899(C;T)

Make rs267606899(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

12848

Gene

ND5

is a	snp
is	mentioned by
dbSNP	rs267606899
dbSNP (classic)	rs267606899
ClinGen	rs267606899
ebi	rs267606899
HLI	rs267606899
Exac	rs267606899
Gnomad	rs267606899
Varsome	rs267606899
LitVar	rs267606899
Map	rs267606899
PheGenI	rs267606899
Biobank	rs267606899
1000 genomes	rs267606899
hgdp	rs267606899
ensembl	rs267606899
geneview	rs267606899
scholar	rs267606899
google	rs267606899
pharmgkb	rs267606899
gwascentral	rs267606899
openSNP	rs267606899
23andMe	rs267606899
SNPshot	rs267606899
SNPdbe	rs267606899
MSV3d	rs267606899
GWAS Ctlg	rs267606899

Max Magnitude

0

ClinVar
Risk	rs267606899(T;T)
Alt	rs267606899(T;T)
Reference	Rs267606899(C;C)
Significance	Pathogenic
Disease	Leber's optic atrophy
Variation	info
Gene	ND5
CLNDBN	Leber's optic atrophy
Reversed	0
HGVS	NC_012920.1:m.12848C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010350.2,