rs587780529

Orientation

plus

Stabilized

plus

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

Make rs587780529(A;A)

Make rs587780529(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

10134

Gene

ND3

is a	snp
is	mentioned by
dbSNP	rs587780529
dbSNP (classic)	rs587780529
ClinGen	rs587780529
ebi	rs587780529
HLI	rs587780529
Exac	rs587780529
Gnomad	rs587780529
Varsome	rs587780529
LitVar	rs587780529
Map	rs587780529
PheGenI	rs587780529
Biobank	rs587780529
1000 genomes	rs587780529
hgdp	rs587780529
ensembl	rs587780529
geneview	rs587780529
scholar	rs587780529
google	rs587780529
pharmgkb	rs587780529
gwascentral	rs587780529
openSNP	rs587780529
23andMe	rs587780529
SNPshot	rs587780529
SNPdbe	rs587780529
MSV3d	rs587780529
GWAS Ctlg	rs587780529

Max Magnitude

0

ClinVar
Risk	rs587780529(A;A)
Alt	rs587780529(A;A)
Reference	Rs587780529(C;C)
Significance	Pathogenic
Disease	Leigh syndrome
Variation	info
Gene	ND3
CLNDBN	Leigh syndrome
Reversed	0
HGVS	NC_012920.1:m.10134C>A
CLNSRC
CLNACC	RCV000144458.1,