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rs863223937

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223937(A;C)
Make rs863223937(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position83264308
GeneCOQ2
is asnp
is mentioned by
dbSNPrs863223937
ebirs863223937
HLIrs863223937
Exacrs863223937
Varsomers863223937
Maprs863223937
PheGenIrs863223937
hapmaprs863223937
1000 genomesrs863223937
hgdprs863223937
ensemblrs863223937
gopubmedrs863223937
geneviewrs863223937
scholarrs863223937
googlers863223937
pharmgkbrs863223937
gwascentralrs863223937
openSNPrs863223937
23andMers863223937
23andMe allrs863223937
SNP Nexus

SNPshotrs863223937
SNPdbers863223937
MSV3drs863223937
GWAS Ctlgrs863223937
Max Magnitude0
ClinVar
Risk rs863223937(C;C)
Alt rs863223937(C;C)
Reference rs863223937(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COQ2
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.84185461T>G
CLNSRC
CLNACC RCV000196578.1,