rs200873900

Orientation

plus

Stabilized

plus

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

Make rs200873900(A;A)

Make rs200873900(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

11696

Gene

ND4

is a	snp
is	mentioned by
dbSNP	rs200873900
dbSNP (classic)	rs200873900
ClinGen	rs200873900
ebi	rs200873900
HLI	rs200873900
Exac	rs200873900
Gnomad	rs200873900
Varsome	rs200873900
LitVar	rs200873900
Map	rs200873900
PheGenI	rs200873900
Biobank	rs200873900
1000 genomes	rs200873900
hgdp	rs200873900
ensembl	rs200873900
geneview	rs200873900
scholar	rs200873900
google	rs200873900
pharmgkb	rs200873900
gwascentral	rs200873900
openSNP	rs200873900
23andMe	rs200873900
SNPshot	rs200873900
SNPdbe	rs200873900
MSV3d	rs200873900
GWAS Ctlg	rs200873900

GMAF

0.008419

Max Magnitude

0

ClinVar
Risk	rs200873900(A;A)
Alt	rs200873900(A;A)
Reference	Rs200873900(G;G)
Significance	Pathogenic
Disease	Leber hereditary optic neuropathy with dystonia Leber's optic atrophy
Variation	info
Gene	ND4
CLNDBN	Leber hereditary optic neuropathy with dystonia Leber's optic atrophy
Reversed	0
HGVS	NC_012920.1:m.11696G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010356.2, RCV000055697.1,