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rs387906489

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906489(-;-)
Make rs387906489(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position11298834
GeneAMELX, ARHGAP6
is asnp
is mentioned by
dbSNPrs387906489
ebirs387906489
HLIrs387906489
Exacrs387906489
Varsomers387906489
Maprs387906489
PheGenIrs387906489
hapmaprs387906489
1000 genomesrs387906489
hgdprs387906489
ensemblrs387906489
gopubmedrs387906489
geneviewrs387906489
scholarrs387906489
googlers387906489
pharmgkbrs387906489
gwascentralrs387906489
openSNPrs387906489
23andMers387906489
23andMe allrs387906489
SNP Nexus

SNPshotrs387906489
SNPdbers387906489
MSV3drs387906489
GWAS Ctlgrs387906489
Max Magnitude0
ClinVar
Risk rs387906489(;)
Alt rs387906489(;)
Reference rs387906489(C;C)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene AMELX ARHGAP6
CLNDBN Amelogenesis imperfecta, type 1E
Reversed 0
HGVS NC_000023.10:g.11316954delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000011889.6,