rs369202065

Orientation

plus

Stabilized

plus

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

Make rs369202065(C;C)

Make rs369202065(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

8839

Gene

ATP6

is a	snp
is	mentioned by
dbSNP	rs369202065
dbSNP (classic)	rs369202065
ClinGen	rs369202065
ebi	rs369202065
HLI	rs369202065
Exac	rs369202065
Gnomad	rs369202065
Varsome	rs369202065
LitVar	rs369202065
Map	rs369202065
PheGenI	rs369202065
Biobank	rs369202065
1000 genomes	rs369202065
hgdp	rs369202065
ensembl	rs369202065
geneview	rs369202065
scholar	rs369202065
google	rs369202065
pharmgkb	rs369202065
gwascentral	rs369202065
openSNP	rs369202065
23andMe	rs369202065
SNPshot	rs369202065
SNPdbe	rs369202065
MSV3d	rs369202065
GWAS Ctlg	rs369202065

Merged from

Rs587776443

Max Magnitude

0

ClinVar
Risk	rs369202065(A;A) rs369202065(C;C)
Alt	rs369202065(A;A) rs369202065(C;C)
Reference	Rs369202065(G;G)
Significance	Pathogenic
Disease	Leigh syndrome
Variation	info
Gene	ATP6
CLNDBN	Leigh syndrome
Reversed	0
HGVS	NC_012920.1:m.8839G>C
CLNSRC
CLNACC	RCV000144024.2,