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rs745688122

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs745688122(C;T)
Make rs745688122(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position95693897
GeneTCTN3
is asnp
is mentioned by
dbSNPrs745688122
ebirs745688122
HLIrs745688122
Exacrs745688122
Varsomers745688122
Maprs745688122
PheGenIrs745688122
hapmaprs745688122
1000 genomesrs745688122
hgdprs745688122
ensemblrs745688122
gopubmedrs745688122
geneviewrs745688122
scholarrs745688122
googlers745688122
pharmgkbrs745688122
gwascentralrs745688122
openSNPrs745688122
23andMers745688122
23andMe allrs745688122
SNP Nexus

SNPshotrs745688122
SNPdbers745688122
MSV3drs745688122
GWAS Ctlgrs745688122
Max Magnitude0
ClinVar
Risk rs745688122(T;T)
Alt rs745688122(T;T)
Reference rs745688122(C;C)
Significance Pathogenic
Disease Joubert syndrome 18
Variation info
Gene TCTN3
CLNDBN Joubert syndrome 18
Reversed 0
HGVS NC_000010.10:g.97453654C>T
CLNSRC
CLNACC RCV000201547.1,