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rs786205897

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205897(-;-)
Make rs786205897(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position57456647
GeneCOQ9
is asnp
is mentioned by
dbSNPrs786205897
ebirs786205897
HLIrs786205897
Exacrs786205897
Varsomers786205897
Maprs786205897
PheGenIrs786205897
hapmaprs786205897
1000 genomesrs786205897
hgdprs786205897
ensemblrs786205897
gopubmedrs786205897
geneviewrs786205897
scholarrs786205897
googlers786205897
pharmgkbrs786205897
gwascentralrs786205897
openSNPrs786205897
23andMers786205897
23andMe allrs786205897
SNP Nexus

SNPshotrs786205897
SNPdbers786205897
MSV3drs786205897
GWAS Ctlgrs786205897
Max Magnitude0
ClinVar
Risk rs786205897(;)
Alt rs786205897(;)
Reference rs786205897(G;G)
Significance Pathogenic
Disease Coenzyme Q10 deficiency
Variation info
Gene COQ9
CLNDBN Coenzyme Q10 deficiency, primary, 5
Reversed 0
HGVS NC_000016.10:g.57456647delG
CLNSRC
CLNACC RCV000172872.1,