rs199795644

Orientation

plus

Stabilized

plus

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

Make rs199795644(A;A)

Make rs199795644(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

14831

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs199795644
dbSNP (classic)	rs199795644
ClinGen	rs199795644
ebi	rs199795644
HLI	rs199795644
Exac	rs199795644
Gnomad	rs199795644
Varsome	rs199795644
LitVar	rs199795644
Map	rs199795644
PheGenI	rs199795644
Biobank	rs199795644
1000 genomes	rs199795644
hgdp	rs199795644
ensembl	rs199795644
geneview	rs199795644
scholar	rs199795644
google	rs199795644
pharmgkb	rs199795644
gwascentral	rs199795644
openSNP	rs199795644
23andMe	rs199795644
SNPshot	rs199795644
SNPdbe	rs199795644
MSV3d	rs199795644
GWAS Ctlg	rs199795644

Max Magnitude

0

ClinVar
Risk	rs199795644(A;A)
Alt	rs199795644(A;A)
Reference	Rs199795644(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.14831G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000055706.1,