rs28616230

Orientation

plus

Stabilized

plus

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

Make rs28616230(A;A)

Make rs28616230(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

4171

Gene

ND1

is a	snp
is	mentioned by
dbSNP	rs28616230
dbSNP (classic)	rs28616230
ClinGen	rs28616230
ebi	rs28616230
HLI	rs28616230
Exac	rs28616230
Gnomad	rs28616230
Varsome	rs28616230
LitVar	rs28616230
Map	rs28616230
PheGenI	rs28616230
Biobank	rs28616230
1000 genomes	rs28616230
hgdp	rs28616230
ensembl	rs28616230
geneview	rs28616230
scholar	rs28616230
google	rs28616230
pharmgkb	rs28616230
gwascentral	rs28616230
openSNP	rs28616230
23andMe	rs28616230
SNPshot	rs28616230
SNPdbe	rs28616230
MSV3d	rs28616230
GWAS Ctlg	rs28616230

Max Magnitude

0

ClinVar
Risk	rs28616230(A;A) rs28616230(T;T)
Alt	rs28616230(A;A) rs28616230(T;T)
Reference	Rs28616230(C;C)
Significance	Pathogenic
Disease	Leber's optic atrophy
Variation	info
Gene	ND1
CLNDBN	Leber's optic atrophy
Reversed	0
HGVS	NC_012920.1:m.4171C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010384.4,