rs267606614

Orientation

plus

Stabilized

plus

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

Make rs267606614(-;C)

Make rs267606614(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

9537

Gene

COX3

is a	snp
is	mentioned by
dbSNP	rs267606614
dbSNP (classic)	rs267606614
ClinGen	rs267606614
ebi	rs267606614
HLI	rs267606614
Exac	rs267606614
Gnomad	rs267606614
Varsome	rs267606614
LitVar	rs267606614
Map	rs267606614
PheGenI	rs267606614
Biobank	rs267606614
1000 genomes	rs267606614
hgdp	rs267606614
ensembl	rs267606614
geneview	rs267606614
scholar	rs267606614
google	rs267606614
pharmgkb	rs267606614
gwascentral	rs267606614
openSNP	rs267606614
23andMe	rs267606614
SNPshot	rs267606614
SNPdbe	rs267606614
MSV3d	rs267606614
GWAS Ctlg	rs267606614

Max Magnitude

0

ClinVar
Risk	rs267606614(C;C)
Alt	rs267606614(C;C)
Reference	Rs267606614(-;-)
Significance	Pathogenic
Disease	Cytochrome-c oxidase deficiency Leigh syndrome
Variation	info
Gene	COX3
CLNDBN	Cytochrome-c oxidase deficiency Leigh syndrome
Reversed	0
HGVS	NC_012920.1:m.9537dupC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010292.2, RCV000144008.2,