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rs793888507

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs793888507(-;-)
Make rs793888507(-;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position95687652
GeneTCTN3
is asnp
is mentioned by
dbSNPrs793888507
ebirs793888507
HLIrs793888507
Exacrs793888507
Varsomers793888507
Maprs793888507
PheGenIrs793888507
hapmaprs793888507
1000 genomesrs793888507
hgdprs793888507
ensemblrs793888507
gopubmedrs793888507
geneviewrs793888507
scholarrs793888507
googlers793888507
pharmgkbrs793888507
gwascentralrs793888507
openSNPrs793888507
23andMers793888507
23andMe allrs793888507
SNP Nexus

SNPshotrs793888507
SNPdbers793888507
MSV3drs793888507
GWAS Ctlgrs793888507
Max Magnitude0
ClinVar
Risk rs793888507(;)
Alt rs793888507(;)
Reference rs793888507(AG;AG)
Significance Pathogenic
Disease Orofacial-digital syndrome IV
Variation info
Gene TCTN3
CLNDBN Orofacial-digital syndrome IV
Reversed 1
HGVS NC_000010.10:g.97447409_97447410delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000030713.5,