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rs1060499551

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499551(-;-)
Make rs1060499551(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position106928175
GeneZNF462
is asnp
is mentioned by
dbSNPrs1060499551
dbSNP (old)rs1060499551
ClinGenrs1060499551
ebirs1060499551
HLIrs1060499551
Exacrs1060499551
Gnomadrs1060499551
Varsomers1060499551
Maprs1060499551
PheGenIrs1060499551
Biobankrs1060499551
1000 genomesrs1060499551
hgdprs1060499551
ensemblrs1060499551
gopubmedrs1060499551
geneviewrs1060499551
scholarrs1060499551
googlers1060499551
pharmgkbrs1060499551
gwascentralrs1060499551
openSNPrs1060499551
23andMers1060499551
23andMe allrs1060499551
SNPshotrs1060499551
SNPdbers1060499551
MSV3drs1060499551
GWAS Ctlgrs1060499551
Max Magnitude0
ClinVar
Risk rs1060499551(-;-)
Alt rs1060499551(-;-)
Reference Rs1060499551(A;A)
Significance Pathogenic
Disease Craniosynostosis Mental retardation
Variation info
Gene ZNF462
CLNDBN Craniosynostosis Mental retardation, autosomal dominant
Reversed 0
HGVS NC_000009.11:g.109690456delA
CLNSRC
CLNACC RCV000450382.1,