rs41518645

Orientation

plus

Stabilized

plus

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

Make rs41518645(A;A)

Make rs41518645(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

15257

Gene

CYTB

is a	snp
is	mentioned by
dbSNP	rs41518645
dbSNP (classic)	rs41518645
ClinGen	rs41518645
ebi	rs41518645
HLI	rs41518645
Exac	rs41518645
Gnomad	rs41518645
Varsome	rs41518645
LitVar	rs41518645
Map	rs41518645
PheGenI	rs41518645
Biobank	rs41518645
1000 genomes	rs41518645
hgdp	rs41518645
ensembl	rs41518645
geneview	rs41518645
scholar	rs41518645
google	rs41518645
pharmgkb	rs41518645
gwascentral	rs41518645
openSNP	rs41518645
23andMe	rs41518645
SNPshot	rs41518645
SNPdbe	rs41518645
MSV3d	rs41518645
GWAS Ctlg	rs41518645

GMAF

0.006548

Max Magnitude

0

ClinVar
Risk	rs41518645(A;A)
Alt	rs41518645(A;A)
Reference	Rs41518645(G;G)
Significance	Other
Disease	Leber's optic atrophy
Variation	info
Gene	CYTB
CLNDBN	Leber's optic atrophy
Reversed	0
HGVS	NC_012920.1:m.15257G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010312.4,