rs587776435

Orientation

plus

Stabilized

plus

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

Make rs587776435(G;G)

Make rs587776435(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

5523

is a	snp
is	mentioned by
dbSNP	rs587776435
dbSNP (classic)	rs587776435
ClinGen	rs587776435
ebi	rs587776435
HLI	rs587776435
Exac	rs587776435
Gnomad	rs587776435
Varsome	rs587776435
LitVar	rs587776435
Map	rs587776435
PheGenI	rs587776435
Biobank	rs587776435
1000 genomes	rs587776435
hgdp	rs587776435
ensembl	rs587776435
geneview	rs587776435
scholar	rs587776435
google	rs587776435
pharmgkb	rs587776435
gwascentral	rs587776435
openSNP	rs587776435
23andMe	rs587776435
SNPshot	rs587776435
SNPdbe	rs587776435
MSV3d	rs587776435
GWAS Ctlg	rs587776435

Max Magnitude

0

ClinVar
Risk	rs587776435(G;G)
Alt	rs587776435(G;G)
Reference	Rs587776435(T;T)
Significance	Pathogenic
Disease	Leigh syndrome
Variation	info
Gene
CLNDBN	Leigh syndrome
Reversed	0
HGVS	NC_012920.1:m.5523T>G
CLNSRC
CLNACC	RCV000144001.2,