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rs134136

From SNPedia

Orientationplus
Stabilizedplus
Make rs134136(C;C)
Make rs134136(C;T)
Make rs134136(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position26503508
GeneTFIP11
is asnp
is mentioned by
dbSNPrs134136
dbSNP (old)rs134136
ClinGenrs134136
ebirs134136
HLIrs134136
Exacrs134136
Gnomadrs134136
Varsomers134136
Maprs134136
PheGenIrs134136
Biobankrs134136
1000 genomesrs134136
hgdprs134136
ensemblrs134136
gopubmedrs134136
geneviewrs134136
scholarrs134136
googlers134136
pharmgkbrs134136
gwascentralrs134136
openSNPrs134136
23andMers134136
23andMe allrs134136
SNPshotrs134136
SNPdbers134136
MSV3drs134136
GWAS Ctlgrs134136
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 28382465OA-icon.png] Significance of genetic variations in developmental enamel defects of primary dentition in Polish children.