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rs768525869

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs768525869(-;-)
Make rs768525869(-;AG)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position95682754
GeneTCTN3
is asnp
is mentioned by
dbSNPrs768525869
ebirs768525869
HLIrs768525869
Exacrs768525869
Varsomers768525869
Maprs768525869
PheGenIrs768525869
hapmaprs768525869
1000 genomesrs768525869
hgdprs768525869
ensemblrs768525869
gopubmedrs768525869
geneviewrs768525869
scholarrs768525869
googlers768525869
pharmgkbrs768525869
gwascentralrs768525869
openSNPrs768525869
23andMers768525869
23andMe allrs768525869
SNP Nexus

SNPshotrs768525869
SNPdbers768525869
MSV3drs768525869
GWAS Ctlgrs768525869
Max Magnitude0
ClinVar
Risk rs768525869(;)
Alt rs768525869(;)
Reference rs768525869(AG;AG)
Significance Pathogenic
Disease Orofacial-digital syndrome IV
Variation info
Gene TCTN3
CLNDBN Orofacial-digital syndrome IV
Reversed 0
HGVS NC_000010.10:g.97442511_97442512delAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000030714.3,