rs118203891

Orientation

plus

Stabilized

plus

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

Make rs118203891(C;C)

Make rs118203891(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

5874

is a	snp
is	mentioned by
dbSNP	rs118203891
dbSNP (classic)	rs118203891
ClinGen	rs118203891
ebi	rs118203891
HLI	rs118203891
Exac	rs118203891
Gnomad	rs118203891
Varsome	rs118203891
LitVar	rs118203891
Map	rs118203891
PheGenI	rs118203891
Biobank	rs118203891
1000 genomes	rs118203891
hgdp	rs118203891
ensembl	rs118203891
geneview	rs118203891
scholar	rs118203891
google	rs118203891
pharmgkb	rs118203891
gwascentral	rs118203891
openSNP	rs118203891
23andMe	rs118203891
SNPshot	rs118203891
SNPdbe	rs118203891
MSV3d	rs118203891
GWAS Ctlg	rs118203891

Max Magnitude

0

ClinVar
Risk	rs118203891(C;C)
Alt	rs118203891(C;C)
Reference	Rs118203891(T;T)
Significance	Pathogenic
Disease	Exercise intolerance and complex III deficiency
Variation	info
Gene
CLNDBN	Exercise intolerance and complex III deficiency, somatic
Reversed	0
HGVS	NC_012920.1:m.5874T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010159.4,