rs869025186

Orientation

plus

Stabilized

plus

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

Make rs869025186(C;C)

Make rs869025186(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

14498

Gene

ND6

is a	snp
is	mentioned by
dbSNP	rs869025186
dbSNP (classic)	rs869025186
ClinGen	rs869025186
ebi	rs869025186
HLI	rs869025186
Exac	rs869025186
Gnomad	rs869025186
Varsome	rs869025186
LitVar	rs869025186
Map	rs869025186
PheGenI	rs869025186
Biobank	rs869025186
1000 genomes	rs869025186
hgdp	rs869025186
ensembl	rs869025186
geneview	rs869025186
scholar	rs869025186
google	rs869025186
pharmgkb	rs869025186
gwascentral	rs869025186
openSNP	rs869025186
23andMe	rs869025186
SNPshot	rs869025186
SNPdbe	rs869025186
MSV3d	rs869025186
GWAS Ctlg	rs869025186

Max Magnitude

0

ClinVar
Risk	rs869025186(C;C)
Alt	rs869025186(C;C)
Reference	Rs869025186(T;T)
Significance	Pathogenic
Disease	Leber's optic atrophy
Variation	info
Gene	ND6
CLNDBN	Leber's optic atrophy
Reversed	0
HGVS	NC_012920.1:m.14498T>C
CLNSRC
CLNACC	RCV000055702.1,