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rs201663231

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201663231(C;G)
Make rs201663231(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position99714620
GeneCOX15
is asnp
is mentioned by
dbSNPrs201663231
ebirs201663231
HLIrs201663231
Exacrs201663231
Varsomers201663231
Maprs201663231
PheGenIrs201663231
hapmaprs201663231
1000 genomesrs201663231
hgdprs201663231
ensemblrs201663231
gopubmedrs201663231
geneviewrs201663231
scholarrs201663231
googlers201663231
pharmgkbrs201663231
gwascentralrs201663231
openSNPrs201663231
23andMers201663231
23andMe allrs201663231
SNP Nexus

SNPshotrs201663231
SNPdbers201663231
MSV3drs201663231
GWAS Ctlgrs201663231
Max Magnitude0
ClinVar
Risk rs201663231(G;G)
Alt rs201663231(G;G)
Reference rs201663231(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COX15
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.101474377C>G
CLNSRC
CLNACC RCV000195737.2,