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rs793888508

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs793888508(A;A)
Make rs793888508(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position95685585
GeneTCTN3
is asnp
is mentioned by
dbSNPrs793888508
ebirs793888508
HLIrs793888508
Exacrs793888508
Varsomers793888508
Maprs793888508
PheGenIrs793888508
hapmaprs793888508
1000 genomesrs793888508
hgdprs793888508
ensemblrs793888508
gopubmedrs793888508
geneviewrs793888508
scholarrs793888508
googlers793888508
pharmgkbrs793888508
gwascentralrs793888508
openSNPrs793888508
23andMers793888508
23andMe allrs793888508
SNP Nexus

SNPshotrs793888508
SNPdbers793888508
MSV3drs793888508
GWAS Ctlgrs793888508
Max Magnitude0
ClinVar
Risk rs793888508(A;A)
Alt rs793888508(A;A)
Reference rs793888508(G;G)
Significance Pathogenic
Disease Joubert syndrome 18
Variation info
Gene TCTN3
CLNDBN Joubert syndrome 18
Reversed 1
HGVS NC_000010.10:g.97445342C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030715.3,