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rs116998555

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs116998555(C;T)
Make rs116998555(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position218890118
GeneWNT10A
is asnp
is mentioned by
dbSNPrs116998555
dbSNP (old)rs116998555
ClinGenrs116998555
ebirs116998555
HLIrs116998555
Exacrs116998555
Gnomadrs116998555
Varsomers116998555
Maprs116998555
PheGenIrs116998555
Biobankrs116998555
1000 genomesrs116998555
hgdprs116998555
ensemblrs116998555
gopubmedrs116998555
geneviewrs116998555
scholarrs116998555
googlers116998555
pharmgkbrs116998555
gwascentralrs116998555
openSNPrs116998555
23andMers116998555
23andMe allrs116998555
SNPshotrs116998555
SNPdbers116998555
MSV3drs116998555
GWAS Ctlgrs116998555
Max Magnitude0
ClinVar
Risk rs116998555(A;A) rs116998555(T;T)
Alt rs116998555(A;A) rs116998555(T;T)
Reference Rs116998555(C;C)
Significance Probable-Pathogenic
Disease not provided Schopf-Schulz-Passarge syndrome Odontoonychodermal dysplasia Selective tooth agenesis Tooth agenesis
Variation info
Gene WNT10A
CLNDBN not provided Schopf-Schulz-Passarge syndrome Odontoonychodermal dysplasia Selective tooth agenesis Tooth agenesis, selective, 4
Reversed 0
HGVS NC_000002.11:g.219754840C>T
CLNSRC Illumina
CLNACC RCV000255246.1, RCV000299227.1, RCV000335291.1, RCV000396415.1, RCV000490286.1,