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rs1060499740

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499740(G;G)
Make rs1060499740(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position102348559
GeneCINP
is asnp
is mentioned by
dbSNPrs1060499740
dbSNP (old)rs1060499740
ClinGenrs1060499740
ebirs1060499740
HLIrs1060499740
Exacrs1060499740
Gnomadrs1060499740
Varsomers1060499740
Maprs1060499740
PheGenIrs1060499740
Biobankrs1060499740
1000 genomesrs1060499740
hgdprs1060499740
ensemblrs1060499740
gopubmedrs1060499740
geneviewrs1060499740
scholarrs1060499740
googlers1060499740
pharmgkbrs1060499740
gwascentralrs1060499740
openSNPrs1060499740
23andMers1060499740
23andMe allrs1060499740
SNPshotrs1060499740
SNPdbers1060499740
MSV3drs1060499740
GWAS Ctlgrs1060499740
Max Magnitude0
ClinVar
Risk rs1060499740(G;G)
Alt rs1060499740(G;G)
Reference Rs1060499740(T;T)
Significance Probable-Pathogenic
Disease Intellectual disability Microcephaly Seizures
Variation info
Gene CINP
CLNDBN Intellectual disability Microcephaly Seizures
Reversed 1
HGVS NC_000014.8:g.102814896A>C
CLNSRC
CLNACC RCV000454213.1,