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rs773943371

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773943371(C;T)
Make rs773943371(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position128325835
GeneCOQ4
is asnp
is mentioned by
dbSNPrs773943371
dbSNP (classic)rs773943371
ClinGenrs773943371
ebirs773943371
HLIrs773943371
Exacrs773943371
Gnomadrs773943371
Varsomers773943371
LitVarrs773943371
Maprs773943371
PheGenIrs773943371
Biobankrs773943371
1000 genomesrs773943371
hgdprs773943371
ensemblrs773943371
geneviewrs773943371
scholarrs773943371
googlers773943371
pharmgkbrs773943371
gwascentralrs773943371
openSNPrs773943371
23andMers773943371
23andMe allrs773943371
SNPshotrs773943371
SNPdbers773943371
MSV3drs773943371
GWAS Ctlgrs773943371
Max Magnitude0
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,