rs199476119

Orientation

plus

Stabilized

plus

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

Make rs199476119(C;C)

Make rs199476119(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

4160

Gene

ND1

is a	snp
is	mentioned by
dbSNP	rs199476119
dbSNP (classic)	rs199476119
ClinGen	rs199476119
ebi	rs199476119
HLI	rs199476119
Exac	rs199476119
Gnomad	rs199476119
Varsome	rs199476119
LitVar	rs199476119
Map	rs199476119
PheGenI	rs199476119
Biobank	rs199476119
1000 genomes	rs199476119
hgdp	rs199476119
ensembl	rs199476119
geneview	rs199476119
scholar	rs199476119
google	rs199476119
pharmgkb	rs199476119
gwascentral	rs199476119
openSNP	rs199476119
23andMe	rs199476119
SNPshot	rs199476119
SNPdbe	rs199476119
MSV3d	rs199476119
GWAS Ctlg	rs199476119

Max Magnitude

0

ClinVar
Risk	rs199476119(C;C)
Alt	rs199476119(C;C)
Reference	Rs199476119(T;T)
Significance	Pathogenic
Disease	Leber's optic atrophy
Variation	info
Gene	ND1
CLNDBN	Leber's optic atrophy
Reversed	0
HGVS	NC_012920.1:m.4160T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010372.2,