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rs387906491

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906491(-;-)
Make rs387906491(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position11298781
GeneAMELX, ARHGAP6
is asnp
is mentioned by
dbSNPrs387906491
ebirs387906491
HLIrs387906491
Exacrs387906491
Varsomers387906491
Maprs387906491
PheGenIrs387906491
hapmaprs387906491
1000 genomesrs387906491
hgdprs387906491
ensemblrs387906491
gopubmedrs387906491
geneviewrs387906491
scholarrs387906491
googlers387906491
pharmgkbrs387906491
gwascentralrs387906491
openSNPrs387906491
23andMers387906491
23andMe allrs387906491
SNP Nexus

SNPshotrs387906491
SNPdbers387906491
MSV3drs387906491
GWAS Ctlgrs387906491
Max Magnitude0
ClinVar
Risk rs387906491(;)
Alt rs387906491(;)
Reference rs387906491(C;C)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene AMELX ARHGAP6
CLNDBN Amelogenesis imperfecta, type 1E
Reversed 0
HGVS NC_000023.10:g.11316901delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000011894.2,