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rs863223944

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223944(A;C)
Make rs863223944(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position99727555
GeneCOX15
is asnp
is mentioned by
dbSNPrs863223944
ebirs863223944
HLIrs863223944
Exacrs863223944
Varsomers863223944
Maprs863223944
PheGenIrs863223944
hapmaprs863223944
1000 genomesrs863223944
hgdprs863223944
ensemblrs863223944
gopubmedrs863223944
geneviewrs863223944
scholarrs863223944
googlers863223944
pharmgkbrs863223944
gwascentralrs863223944
openSNPrs863223944
23andMers863223944
23andMe allrs863223944
SNP Nexus

SNPshotrs863223944
SNPdbers863223944
MSV3drs863223944
GWAS Ctlgrs863223944
Max Magnitude0
ClinVar
Risk rs863223944(C;C)
Alt rs863223944(C;C)
Reference rs863223944(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COX15
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.101487312T>G
CLNSRC
CLNACC RCV000197734.1,