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rs201908721

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201908721(C;T)
Make rs201908721(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position226982719
GeneADCK3, COQ8A
is asnp
is mentioned by
dbSNPrs201908721
dbSNP (classic)rs201908721
ClinGenrs201908721
ebirs201908721
HLIrs201908721
Exacrs201908721
Gnomadrs201908721
Varsomers201908721
LitVarrs201908721
Maprs201908721
PheGenIrs201908721
Biobankrs201908721
1000 genomesrs201908721
hgdprs201908721
ensemblrs201908721
geneviewrs201908721
scholarrs201908721
googlers201908721
pharmgkbrs201908721
gwascentralrs201908721
openSNPrs201908721
23andMers201908721
SNPshotrs201908721
SNPdbers201908721
MSV3drs201908721
GWAS Ctlgrs201908721
Max Magnitude0
ClinVar
Risk rs201908721(T;T)
Alt rs201908721(T;T)
Reference Rs201908721(C;C)
Significance Pathogenic
Disease not provided Coenzyme Q10 deficiency
Variation info
Gene COQ8A ADCK3
CLNDBN not provided Coenzyme Q10 deficiency, primary, 4
Reversed 0
HGVS NC_000001.10:g.227170420C>T
CLNSRC
CLNACC RCV000413531.1, RCV000416388.1,