rs267606893

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	Ancestry miscall in all likelihood
(T;T)	0	common in clinvar

Make rs267606893(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

12706

Gene

ND5

is a	snp
is	mentioned by
dbSNP	rs267606893
dbSNP (classic)	rs267606893
ClinGen	rs267606893
ebi	rs267606893
HLI	rs267606893
Exac	rs267606893
Gnomad	rs267606893
Varsome	rs267606893
LitVar	rs267606893
Map	rs267606893
PheGenI	rs267606893
Biobank	rs267606893
1000 genomes	rs267606893
hgdp	rs267606893
ensembl	rs267606893
geneview	rs267606893
scholar	rs267606893
google	rs267606893
pharmgkb	rs267606893
gwascentral	rs267606893
openSNP	rs267606893
23andMe	rs267606893
SNPshot	rs267606893
SNPdbe	rs267606893
MSV3d	rs267606893
GWAS Ctlg	rs267606893

Merged from

Rs2854122

Max Magnitude

0

ClinVar
Risk	Rs267606893(C;C)
Alt	Rs267606893(C;C)
Reference	Rs267606893(T;T)
Significance	Pathogenic
Disease	Leigh syndrome due to mitochondrial complex I deficiency Leigh syndrome
Variation	info
Gene	ND5
CLNDBN	Leigh syndrome due to mitochondrial complex I deficiency Leigh syndrome
Reversed	0
HGVS	NC_012920.1:m.12706T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010338.2, RCV000144015.2,