rs387906426

Orientation

plus

Stabilized

plus

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

Make rs387906426(A;A)

Make rs387906426(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

4640

Gene

ND2

is a	snp
is	mentioned by
dbSNP	rs387906426
dbSNP (classic)	rs387906426
ClinGen	rs387906426
ebi	rs387906426
HLI	rs387906426
Exac	rs387906426
Gnomad	rs387906426
Varsome	rs387906426
LitVar	rs387906426
Map	rs387906426
PheGenI	rs387906426
Biobank	rs387906426
1000 genomes	rs387906426
hgdp	rs387906426
ensembl	rs387906426
geneview	rs387906426
scholar	rs387906426
google	rs387906426
pharmgkb	rs387906426
gwascentral	rs387906426
openSNP	rs387906426
23andMe	rs387906426
SNPshot	rs387906426
SNPdbe	rs387906426
MSV3d	rs387906426
GWAS Ctlg	rs387906426

Max Magnitude

0

ClinVar
Risk	rs387906426(A;A)
Alt	rs387906426(A;A)
Reference	Rs387906426(C;C)
Significance	Pathogenic
Disease	Leber's optic atrophy
Variation	info
Gene	ND2
CLNDBN	Leber's optic atrophy
Reversed	0
HGVS	NC_012920.1:m.4640C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010366.2,