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rs1060499745

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499745(C;G)
Make rs1060499745(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89694721
GeneCDK10
is asnp
is mentioned by
dbSNPrs1060499745
dbSNP (old)rs1060499745
ClinGenrs1060499745
ebirs1060499745
HLIrs1060499745
Exacrs1060499745
Gnomadrs1060499745
Varsomers1060499745
Maprs1060499745
PheGenIrs1060499745
Biobankrs1060499745
1000 genomesrs1060499745
hgdprs1060499745
ensemblrs1060499745
gopubmedrs1060499745
geneviewrs1060499745
scholarrs1060499745
googlers1060499745
pharmgkbrs1060499745
gwascentralrs1060499745
openSNPrs1060499745
23andMers1060499745
23andMe allrs1060499745
SNPshotrs1060499745
SNPdbers1060499745
MSV3drs1060499745
GWAS Ctlgrs1060499745
Max Magnitude0
ClinVar
Risk rs1060499745(G;G)
Alt rs1060499745(G;G)
Reference Rs1060499745(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene CDK10
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000016.9:g.89761129C>G
CLNSRC
CLNACC RCV000454194.1,