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rs368918847

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368918847(C;T)
Make rs368918847(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position14207106
GeneCOX10
is asnp
is mentioned by
dbSNPrs368918847
dbSNP (classic)rs368918847
ClinGenrs368918847
ebirs368918847
HLIrs368918847
Exacrs368918847
Gnomadrs368918847
Varsomers368918847
LitVarrs368918847
Maprs368918847
PheGenIrs368918847
Biobankrs368918847
1000 genomesrs368918847
hgdprs368918847
ensemblrs368918847
geneviewrs368918847
scholarrs368918847
googlers368918847
pharmgkbrs368918847
gwascentralrs368918847
openSNPrs368918847
23andMers368918847
SNPshotrs368918847
SNPdbers368918847
MSV3drs368918847
GWAS Ctlgrs368918847
Max Magnitude0
ClinVar
Risk rs368918847(A;A) rs368918847(T;T)
Alt rs368918847(A;A) rs368918847(T;T)
Reference Rs368918847(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COX10
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.14110423C>T
CLNSRC
CLNACC RCV000479216.1,