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rs387906490

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906490(-;-)
Make rs387906490(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position11298902
GeneAMELX, ARHGAP6
is asnp
is mentioned by
dbSNPrs387906490
ebirs387906490
HLIrs387906490
Exacrs387906490
Varsomers387906490
Maprs387906490
PheGenIrs387906490
hapmaprs387906490
1000 genomesrs387906490
hgdprs387906490
ensemblrs387906490
gopubmedrs387906490
geneviewrs387906490
scholarrs387906490
googlers387906490
pharmgkbrs387906490
gwascentralrs387906490
openSNPrs387906490
23andMers387906490
23andMe allrs387906490
SNP Nexus

SNPshotrs387906490
SNPdbers387906490
MSV3drs387906490
GWAS Ctlgrs387906490
Max Magnitude0
ClinVar
Risk rs387906490(;)
Alt rs387906490(;)
Reference rs387906490(C;C)
Significance Pathogenic
Disease Amelogenesis imperfecta
Variation info
Gene AMELX ARHGAP6
CLNDBN Amelogenesis imperfecta, type 1E
Reversed 0
HGVS NC_000023.10:g.11317022delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000011893.17,