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rs387907273

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907273(C;T)
Make rs387907273(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position95682776
GeneTCTN3
is asnp
is mentioned by
dbSNPrs387907273
ebirs387907273
HLIrs387907273
Exacrs387907273
Varsomers387907273
Maprs387907273
PheGenIrs387907273
hapmaprs387907273
1000 genomesrs387907273
hgdprs387907273
ensemblrs387907273
gopubmedrs387907273
geneviewrs387907273
scholarrs387907273
googlers387907273
pharmgkbrs387907273
gwascentralrs387907273
openSNPrs387907273
23andMers387907273
23andMe allrs387907273
SNP Nexus

SNPshotrs387907273
SNPdbers387907273
MSV3drs387907273
GWAS Ctlgrs387907273
Max Magnitude0
ClinVar
Risk rs387907273(T;T)
Alt rs387907273(T;T)
Reference rs387907273(C;C)
Significance Pathogenic
Disease Orofacial-digital syndrome IV
Variation info
Gene TCTN3
CLNDBN Orofacial-digital syndrome IV
Reversed 1
HGVS NC_000010.10:g.97442533G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030712.2,