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rs1060499549

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499549(C;T)
Make rs1060499549(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position106927699
GeneZNF462
is asnp
is mentioned by
dbSNPrs1060499549
dbSNP (old)rs1060499549
ClinGenrs1060499549
ebirs1060499549
HLIrs1060499549
Exacrs1060499549
Gnomadrs1060499549
Varsomers1060499549
Maprs1060499549
PheGenIrs1060499549
Biobankrs1060499549
1000 genomesrs1060499549
hgdprs1060499549
ensemblrs1060499549
gopubmedrs1060499549
geneviewrs1060499549
scholarrs1060499549
googlers1060499549
pharmgkbrs1060499549
gwascentralrs1060499549
openSNPrs1060499549
23andMers1060499549
23andMe allrs1060499549
SNPshotrs1060499549
SNPdbers1060499549
MSV3drs1060499549
GWAS Ctlgrs1060499549
Max Magnitude0
ClinVar
Risk rs1060499549(T;T)
Alt rs1060499549(T;T)
Reference Rs1060499549(C;C)
Significance Pathogenic
Disease Craniosynostosis Mental retardation
Variation info
Gene ZNF462
CLNDBN Craniosynostosis Mental retardation, autosomal dominant
Reversed 0
HGVS NC_000009.11:g.109689980C>T
CLNSRC
CLNACC RCV000449793.1,