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rs387906487

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906487(-;-)
Make rs387906487(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position11298246
GeneAMELX, ARHGAP6
is asnp
is mentioned by
dbSNPrs387906487
ebirs387906487
HLIrs387906487
Exacrs387906487
Varsomers387906487
Maprs387906487
PheGenIrs387906487
hapmaprs387906487
1000 genomesrs387906487
hgdprs387906487
ensemblrs387906487
gopubmedrs387906487
geneviewrs387906487
scholarrs387906487
googlers387906487
pharmgkbrs387906487
gwascentralrs387906487
openSNPrs387906487
23andMers387906487
23andMe allrs387906487
SNP Nexus

SNPshotrs387906487
SNPdbers387906487
MSV3drs387906487
GWAS Ctlgrs387906487
Max Magnitude0
ClinVar
Risk rs387906487(;)
Alt rs387906487(;)
Reference rs387906487(C;C)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene AMELX ARHGAP6
CLNDBN Amelogenesis imperfecta, type 1E
Reversed 0
HGVS NC_000023.10:g.11316366delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000011887.2,