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rs779410126

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs779410126(-;T)
Make rs779410126(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position135463145
GeneAHI1
is asnp
is mentioned by
dbSNPrs779410126
dbSNP (old)rs779410126
ClinGenrs779410126
ebirs779410126
HLIrs779410126
Exacrs779410126
Gnomadrs779410126
Varsomers779410126
Maprs779410126
PheGenIrs779410126
Biobankrs779410126
1000 genomesrs779410126
hgdprs779410126
ensemblrs779410126
gopubmedrs779410126
geneviewrs779410126
scholarrs779410126
googlers779410126
pharmgkbrs779410126
gwascentralrs779410126
openSNPrs779410126
23andMers779410126
23andMe allrs779410126
SNP Nexus

SNPshotrs779410126
SNPdbers779410126
MSV3drs779410126
GWAS Ctlgrs779410126
Max Magnitude0
ClinVar
Risk rs779410126(T;T)
Alt rs779410126(T;T)
Reference Rs779410126(-;-)
Significance Pathogenic
Disease Joubert syndrome 3
Variation info
Gene AHI1
CLNDBN Joubert syndrome 3
Reversed 0
HGVS NC_000006.11:g.135784284dupT
CLNSRC
CLNACC RCV000201689.1,