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rs387906793

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906793(G;T)
Make rs387906793(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position47417274
GeneFOXE3
is asnp
is mentioned by
dbSNPrs387906793
ebirs387906793
HLIrs387906793
Exacrs387906793
Varsomers387906793
Maprs387906793
PheGenIrs387906793
hapmaprs387906793
1000 genomesrs387906793
hgdprs387906793
ensemblrs387906793
gopubmedrs387906793
geneviewrs387906793
scholarrs387906793
googlers387906793
pharmgkbrs387906793
gwascentralrs387906793
openSNPrs387906793
23andMers387906793
23andMe allrs387906793
SNP Nexus

SNPshotrs387906793
SNPdbers387906793
MSV3drs387906793
GWAS Ctlgrs387906793
Max Magnitude0
ClinVar
Risk rs387906793(T;T)
Alt rs387906793(T;T)
Reference rs387906793(G;G)
Significance Pathogenic
Disease Anterior segment mesenchymal dysgenesis
Variation info
Gene FOXE3
CLNDBN Anterior segment mesenchymal dysgenesis
Reversed 0
HGVS NC_000001.10:g.47882946G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023071.3,