Have questions? Visit https://www.reddit.com/r/SNPedia

rs143441644

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs143441644(C;T)
Make rs143441644(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position128333565
GeneCOQ4
is asnp
is mentioned by
dbSNPrs143441644
ebirs143441644
HLIrs143441644
Exacrs143441644
Varsomers143441644
Maprs143441644
PheGenIrs143441644
hapmaprs143441644
1000 genomesrs143441644
hgdprs143441644
ensemblrs143441644
gopubmedrs143441644
geneviewrs143441644
scholarrs143441644
googlers143441644
pharmgkbrs143441644
gwascentralrs143441644
openSNPrs143441644
23andMers143441644
23andMe allrs143441644
SNP Nexus

SNPshotrs143441644
SNPdbers143441644
MSV3drs143441644
GWAS Ctlgrs143441644
Max Magnitude0
ClinVar
Risk rs143441644(T;T)
Alt rs143441644(T;T)
Reference rs143441644(C;C)
Significance Pathogenic
Disease Coenzyme Q10 deficiency
Variation info
Gene COQ4
CLNDBN Coenzyme Q10 deficiency, primary, 7
Reversed 0
HGVS NC_000009.11:g.131095844C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000169636.3,