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rs17878486

From SNPedia

Orientationplus
Stabilizedplus
Make rs17878486(C;C)
Make rs17878486(C;T)
Make rs17878486(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position11295828
GeneAMELX, ARHGAP6
is asnp
is mentioned by
dbSNPrs17878486
dbSNP (old)rs17878486
ClinGenrs17878486
ebirs17878486
HLIrs17878486
Exacrs17878486
Gnomadrs17878486
Varsomers17878486
Maprs17878486
PheGenIrs17878486
Biobankrs17878486
1000 genomesrs17878486
hgdprs17878486
ensemblrs17878486
gopubmedrs17878486
geneviewrs17878486
scholarrs17878486
googlers17878486
pharmgkbrs17878486
gwascentralrs17878486
openSNPrs17878486
23andMers17878486
23andMe allrs17878486
SNPshotrs17878486
SNPdbers17878486
MSV3drs17878486
GWAS Ctlgrs17878486
Max Magnitude

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