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rs772989270

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs772989270(A;A)
Make rs772989270(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position135438399
GeneAHI1
is asnp
is mentioned by
dbSNPrs772989270
ebirs772989270
HLIrs772989270
Exacrs772989270
Varsomers772989270
Maprs772989270
PheGenIrs772989270
hapmaprs772989270
1000 genomesrs772989270
hgdprs772989270
ensemblrs772989270
gopubmedrs772989270
geneviewrs772989270
scholarrs772989270
googlers772989270
pharmgkbrs772989270
gwascentralrs772989270
openSNPrs772989270
23andMers772989270
23andMe allrs772989270
SNP Nexus

SNPshotrs772989270
SNPdbers772989270
MSV3drs772989270
GWAS Ctlgrs772989270
Max Magnitude0
ClinVar
Risk rs772989270(A;A)
Alt rs772989270(A;A)
Reference rs772989270(G;G)
Significance Pathogenic
Disease Joubert syndrome 3
Variation info
Gene AHI1
CLNDBN Joubert syndrome 3
Reversed 0
HGVS NC_000006.11:g.135759537G>A
CLNSRC
CLNACC RCV000201635.1,