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rs863223942

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223942(C;C)
Make rs863223942(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position99714639
GeneCOX15
is asnp
is mentioned by
dbSNPrs863223942
ebirs863223942
HLIrs863223942
Exacrs863223942
Varsomers863223942
Maprs863223942
PheGenIrs863223942
hapmaprs863223942
1000 genomesrs863223942
hgdprs863223942
ensemblrs863223942
gopubmedrs863223942
geneviewrs863223942
scholarrs863223942
googlers863223942
pharmgkbrs863223942
gwascentralrs863223942
openSNPrs863223942
23andMers863223942
23andMe allrs863223942
SNP Nexus

SNPshotrs863223942
SNPdbers863223942
MSV3drs863223942
GWAS Ctlgrs863223942
Max Magnitude0
ClinVar
Risk rs863223942(C;C)
Alt rs863223942(C;C)
Reference rs863223942(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COX15
CLNDBN not provided
Reversed 1
HGVS NC_000010.10:g.101474396A>G
CLNSRC
CLNACC RCV000199309.1,