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rs764091969

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs764091969(A;A)
Make rs764091969(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position95686506
GeneTCTN3
is asnp
is mentioned by
dbSNPrs764091969
ebirs764091969
HLIrs764091969
Exacrs764091969
Varsomers764091969
Maprs764091969
PheGenIrs764091969
hapmaprs764091969
1000 genomesrs764091969
hgdprs764091969
ensemblrs764091969
gopubmedrs764091969
geneviewrs764091969
scholarrs764091969
googlers764091969
pharmgkbrs764091969
gwascentralrs764091969
openSNPrs764091969
23andMers764091969
23andMe allrs764091969
SNP Nexus

SNPshotrs764091969
SNPdbers764091969
MSV3drs764091969
GWAS Ctlgrs764091969
Max Magnitude0
ClinVar
Risk rs764091969(A;A)
Alt rs764091969(A;A)
Reference rs764091969(G;G)
Significance Pathogenic
Disease Orofacial-digital syndrome IV
Variation info
Gene TCTN3
CLNDBN Orofacial-digital syndrome IV
Reversed 0
HGVS NC_000010.10:g.97446263G>A
CLNSRC
CLNACC RCV000190630.1,