rs200336777

Orientation

plus

Stabilized

plus

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

Make rs200336777(A;A)

Make rs200336777(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15812

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs200336777
dbSNP (classic)	rs200336777
ClinGen	rs200336777
ebi	rs200336777
HLI	rs200336777
Exac	rs200336777
Gnomad	rs200336777
Varsome	rs200336777
LitVar	rs200336777
Map	rs200336777
PheGenI	rs200336777
Biobank	rs200336777
1000 genomes	rs200336777
hgdp	rs200336777
ensembl	rs200336777
geneview	rs200336777
scholar	rs200336777
google	rs200336777
pharmgkb	rs200336777
gwascentral	rs200336777
openSNP	rs200336777
23andMe	rs200336777
SNPshot	rs200336777
SNPdbe	rs200336777
MSV3d	rs200336777
GWAS Ctlg	rs200336777

GMAF

0.005613

Max Magnitude

0

ClinVar
Risk	rs200336777(A;A)
Alt	rs200336777(A;A)
Reference	Rs200336777(G;G)
Significance	Pathogenic
Disease	Leber's optic atrophy
Variation	info
Gene	CYTB
CLNDBN	Leber's optic atrophy
Reversed	0
HGVS	NC_012920.1:m.15812G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010313.4,