rs773943371

Orientation

plus

Stabilized

plus

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

Make rs773943371(C;T)

Make rs773943371(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

128325835

Gene

COQ4

is a	snp
is	mentioned by
dbSNP	rs773943371
dbSNP (classic)	rs773943371
ClinGen	rs773943371
ebi	rs773943371
HLI	rs773943371
Exac	rs773943371
Gnomad	rs773943371
Varsome	rs773943371
LitVar	rs773943371
Map	rs773943371
PheGenI	rs773943371
Biobank	rs773943371
1000 genomes	rs773943371
hgdp	rs773943371
ensembl	rs773943371
geneview	rs773943371
scholar	rs773943371
google	rs773943371
pharmgkb	rs773943371
gwascentral	rs773943371
openSNP	rs773943371
23andMe	rs773943371
SNPshot	rs773943371
SNPdbe	rs773943371
MSV3d	rs773943371
GWAS Ctlg	rs773943371

Max Magnitude

0

ClinVar
Risk	rs773943371(T;T)
Alt	rs773943371(T;T)
Reference	Rs773943371(C;C)
Significance	Pathogenic
Disease	not provided Coenzyme Q10 deficiency
Variation	info
Gene	COQ4
CLNDBN	not provided Coenzyme Q10 deficiency, primary, 7
Reversed	0
HGVS	NC_000009.11:g.131088114C>T
CLNSRC
CLNACC	RCV000438211.1, RCV000477704.1,