rs587776442

Orientation

plus

Stabilized

plus

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

Make rs587776442(C;C)

Make rs587776442(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

3928

Gene

ND1

is a	snp
is	mentioned by
dbSNP	rs587776442
dbSNP (classic)	rs587776442
ClinGen	rs587776442
ebi	rs587776442
HLI	rs587776442
Exac	rs587776442
Gnomad	rs587776442
Varsome	rs587776442
LitVar	rs587776442
Map	rs587776442
PheGenI	rs587776442
Biobank	rs587776442
1000 genomes	rs587776442
hgdp	rs587776442
ensembl	rs587776442
geneview	rs587776442
scholar	rs587776442
google	rs587776442
pharmgkb	rs587776442
gwascentral	rs587776442
openSNP	rs587776442
23andMe	rs587776442
SNPshot	rs587776442
SNPdbe	rs587776442
MSV3d	rs587776442
GWAS Ctlg	rs587776442

Max Magnitude

0

ClinVar
Risk	rs587776442(C;C)
Alt	rs587776442(C;C)
Reference	Rs587776442(G;G)
Significance	Pathogenic
Disease	Leigh syndrome
Variation	info
Gene	ND1
CLNDBN	Leigh syndrome
Reversed	0
HGVS	NC_012920.1:m.3928G>C
CLNSRC
CLNACC	RCV000144023.2,