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rs774395996

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774395996(C;T)
Make rs774395996(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position128332183
GeneCOQ4
is asnp
is mentioned by
dbSNPrs774395996
ebirs774395996
HLIrs774395996
Exacrs774395996
Varsomers774395996
Maprs774395996
PheGenIrs774395996
hapmaprs774395996
1000 genomesrs774395996
hgdprs774395996
ensemblrs774395996
gopubmedrs774395996
geneviewrs774395996
scholarrs774395996
googlers774395996
pharmgkbrs774395996
gwascentralrs774395996
openSNPrs774395996
23andMers774395996
23andMe allrs774395996
SNP Nexus

SNPshotrs774395996
SNPdbers774395996
MSV3drs774395996
GWAS Ctlgrs774395996
Max Magnitude0
ClinVar
Risk rs774395996(G,T;G,T)
Alt rs774395996(G,T;G,T)
Reference rs774395996(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.131094462C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000169634.3,