rs267606913

Orientation

plus

Stabilized

plus

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

Make rs267606913(A;A)

Make rs267606913(A;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

1815885

Gene

NDUFS6

is a	snp
is	mentioned by
dbSNP	rs267606913
dbSNP (classic)	rs267606913
ClinGen	rs267606913
ebi	rs267606913
HLI	rs267606913
Exac	rs267606913
Gnomad	rs267606913
Varsome	rs267606913
LitVar	rs267606913
Map	rs267606913
PheGenI	rs267606913
Biobank	rs267606913
1000 genomes	rs267606913
hgdp	rs267606913
ensembl	rs267606913
geneview	rs267606913
scholar	rs267606913
google	rs267606913
pharmgkb	rs267606913
gwascentral	rs267606913
openSNP	rs267606913
23andMe	rs267606913
SNPshot	rs267606913
SNPdbe	rs267606913
MSV3d	rs267606913
GWAS Ctlg	rs267606913

Max Magnitude

0

ClinVar
Risk	rs267606913(A;A)
Alt	rs267606913(A;A)
Reference	Rs267606913(G;G)
Significance	Pathogenic
Disease	Mitochondrial complex I deficiency
Variation	info
Gene	NDUFS6
CLNDBN	Mitochondrial complex I deficiency
Reversed	0
HGVS	NC_000005.9:g.1815999G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006389.4,