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rs1060499588

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499588(C;T)
Make rs1060499588(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position218890223
GeneWNT10A
is asnp
is mentioned by
dbSNPrs1060499588
dbSNP (old)rs1060499588
ClinGenrs1060499588
ebirs1060499588
HLIrs1060499588
Exacrs1060499588
Gnomadrs1060499588
Varsomers1060499588
Maprs1060499588
PheGenIrs1060499588
Biobankrs1060499588
1000 genomesrs1060499588
hgdprs1060499588
ensemblrs1060499588
gopubmedrs1060499588
geneviewrs1060499588
scholarrs1060499588
googlers1060499588
pharmgkbrs1060499588
gwascentralrs1060499588
openSNPrs1060499588
23andMers1060499588
23andMe allrs1060499588
SNPshotrs1060499588
SNPdbers1060499588
MSV3drs1060499588
GWAS Ctlgrs1060499588
Max Magnitude0
ClinVar
Risk rs1060499588(T;T)
Alt rs1060499588(T;T)
Reference Rs1060499588(C;C)
Significance Probable-Pathogenic
Disease Odontoonychodermal dysplasia Schopf-Schulz-Passarge syndrome Tooth agenesis
Variation info
Gene WNT10A
CLNDBN Odontoonychodermal dysplasia Schopf-Schulz-Passarge syndrome Tooth agenesis, selective, 4
Reversed 0
HGVS NC_000002.11:g.219754945C>T
CLNSRC
CLNACC RCV000477883.1,