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rs1060499550

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs1060499550(A;A)
Make rs1060499550(A;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position106926891
GeneZNF462
is asnp
is mentioned by
dbSNPrs1060499550
dbSNP (old)rs1060499550
ClinGenrs1060499550
ebirs1060499550
HLIrs1060499550
Exacrs1060499550
Gnomadrs1060499550
Varsomers1060499550
Maprs1060499550
PheGenIrs1060499550
Biobankrs1060499550
1000 genomesrs1060499550
hgdprs1060499550
ensemblrs1060499550
gopubmedrs1060499550
geneviewrs1060499550
scholarrs1060499550
googlers1060499550
pharmgkbrs1060499550
gwascentralrs1060499550
openSNPrs1060499550
23andMers1060499550
23andMe allrs1060499550
SNPshotrs1060499550
SNPdbers1060499550
MSV3drs1060499550
GWAS Ctlgrs1060499550
Max Magnitude0
ClinVar
Risk rs1060499550(A;A)
Alt rs1060499550(A;A)
Reference Rs1060499550(TG;TG)
Significance Pathogenic
Disease Craniosynostosis Mental retardation
Variation info
Gene ZNF462
CLNDBN Craniosynostosis Mental retardation, autosomal dominant
Reversed 0
HGVS NC_000009.11:g.109689172_109689173delTGinsA
CLNSRC
CLNACC RCV000451535.1,