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rs387906405

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGGG;GGGG) 0 common in clinvar
Make rs387906405(-;-)
Make rs387906405(-;GGGG)
ReferenceGRCh38 38.1/141
Chromosome17
Position49991807
GeneDLX3
is asnp
is mentioned by
dbSNPrs387906405
ebirs387906405
HLIrs387906405
Exacrs387906405
Varsomers387906405
Maprs387906405
PheGenIrs387906405
hapmaprs387906405
1000 genomesrs387906405
hgdprs387906405
ensemblrs387906405
gopubmedrs387906405
geneviewrs387906405
scholarrs387906405
googlers387906405
pharmgkbrs387906405
gwascentralrs387906405
openSNPrs387906405
23andMers387906405
23andMe allrs387906405
SNP Nexus

SNPshotrs387906405
SNPdbers387906405
MSV3drs387906405
GWAS Ctlgrs387906405
Max Magnitude0
ClinVar
Risk rs387906405(;)
Alt rs387906405(;)
Reference rs387906405(GGGG;GGGG)
Significance Pathogenic
Disease Tricho-dento-osseous syndrome
Variation info
Gene DLX3
CLNDBN Tricho-dento-osseous syndrome
Reversed 1
HGVS NC_000017.10:g.48069171_48069174delCCCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000009639.1,