rs587776444

Orientation

plus

Stabilized

plus

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

Make rs587776444(C;C)

Make rs587776444(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

8989

Gene

ATP6

is a	snp
is	mentioned by
dbSNP	rs587776444
dbSNP (classic)	rs587776444
ClinGen	rs587776444
ebi	rs587776444
HLI	rs587776444
Exac	rs587776444
Gnomad	rs587776444
Varsome	rs587776444
LitVar	rs587776444
Map	rs587776444
PheGenI	rs587776444
Biobank	rs587776444
1000 genomes	rs587776444
hgdp	rs587776444
ensembl	rs587776444
geneview	rs587776444
scholar	rs587776444
google	rs587776444
pharmgkb	rs587776444
gwascentral	rs587776444
openSNP	rs587776444
23andMe	rs587776444
SNPshot	rs587776444
SNPdbe	rs587776444
MSV3d	rs587776444
GWAS Ctlg	rs587776444

Max Magnitude

0

ClinVar
Risk	rs587776444(C;C)
Alt	rs587776444(C;C)
Reference	Rs587776444(G;G)
Significance	Pathogenic
Disease	Leigh syndrome
Variation	info
Gene	ATP6
CLNDBN	Leigh syndrome
Reversed	0
HGVS	NC_012920.1:m.8989G>C
CLNSRC
CLNACC	RCV000144025.2,