rs869025187

Orientation

plus

Stabilized

plus

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

Make rs869025187(A;A)

Make rs869025187(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

14279

Gene

ND6

is a	snp
is	mentioned by
dbSNP	rs869025187
dbSNP (classic)	rs869025187
ClinGen	rs869025187
ebi	rs869025187
HLI	rs869025187
Exac	rs869025187
Gnomad	rs869025187
Varsome	rs869025187
LitVar	rs869025187
Map	rs869025187
PheGenI	rs869025187
Biobank	rs869025187
1000 genomes	rs869025187
hgdp	rs869025187
ensembl	rs869025187
geneview	rs869025187
scholar	rs869025187
google	rs869025187
pharmgkb	rs869025187
gwascentral	rs869025187
openSNP	rs869025187
23andMe	rs869025187
SNPshot	rs869025187
SNPdbe	rs869025187
MSV3d	rs869025187
GWAS Ctlg	rs869025187

Max Magnitude

0

ClinVar
Risk	rs869025187(A;A)
Alt	rs869025187(A;A)
Reference	Rs869025187(G;G)
Significance	Pathogenic
Disease	Leber's optic atrophy
Variation	info
Gene	ND6
CLNDBN	Leber's optic atrophy
Reversed	0
HGVS	NC_012920.1:m.14279G>A
CLNSRC
CLNACC	RCV000055705.1,