Have questions? Visit https://www.reddit.com/r/SNPedia

rs863225137

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225137(A;A)
Make rs863225137(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position135448289
GeneAHI1
is asnp
is mentioned by
dbSNPrs863225137
ebirs863225137
HLIrs863225137
Exacrs863225137
Varsomers863225137
Maprs863225137
PheGenIrs863225137
hapmaprs863225137
1000 genomesrs863225137
hgdprs863225137
ensemblrs863225137
gopubmedrs863225137
geneviewrs863225137
scholarrs863225137
googlers863225137
pharmgkbrs863225137
gwascentralrs863225137
openSNPrs863225137
23andMers863225137
23andMe allrs863225137
SNP Nexus

SNPshotrs863225137
SNPdbers863225137
MSV3drs863225137
GWAS Ctlgrs863225137
Max Magnitude0
ClinVar
Risk rs863225137(A;A)
Alt rs863225137(A;A)
Reference rs863225137(G;G)
Significance Pathogenic
Disease Joubert syndrome 3
Variation info
Gene AHI1
CLNDBN Joubert syndrome 3
Reversed 1
HGVS NC_000006.11:g.135769427C>T
CLNSRC
CLNACC RCV000201568.1,