rs104894270

Orientation

plus

Stabilized

plus

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

Make rs104894270(C;T)

Make rs104894270(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

47582436

Gene

NDUFS3

is a	snp
is	mentioned by
dbSNP	rs104894270
dbSNP (classic)	rs104894270
ClinGen	rs104894270
ebi	rs104894270
HLI	rs104894270
Exac	rs104894270
Gnomad	rs104894270
Varsome	rs104894270
LitVar	rs104894270
Map	rs104894270
PheGenI	rs104894270
Biobank	rs104894270
1000 genomes	rs104894270
hgdp	rs104894270
ensembl	rs104894270
geneview	rs104894270
scholar	rs104894270
google	rs104894270
pharmgkb	rs104894270
gwascentral	rs104894270
openSNP	rs104894270
23andMe	rs104894270
SNPshot	rs104894270
SNPdbe	rs104894270
MSV3d	rs104894270
GWAS Ctlg	rs104894270

Max Magnitude

0

OMIM	603846
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104894270(T;T)
Alt	rs104894270(T;T)
Reference	Rs104894270(C;C)
Significance	Pathogenic
Disease	Leigh syndrome due to mitochondrial complex I deficiency Mitochondrial complex I deficiency
Variation	info
Gene	NDUFS3
CLNDBN	Leigh syndrome due to mitochondrial complex I deficiency Mitochondrial complex I deficiency
Reversed	0
HGVS	NC_000011.9:g.47603988C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006391.3, RCV000033058.3,