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

rs863225131

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225131(G;G)
Make rs863225131(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position135428757
GeneAHI1
is asnp
is mentioned by
dbSNPrs863225131
ebirs863225131
HLIrs863225131
Exacrs863225131
Varsomers863225131
Maprs863225131
PheGenIrs863225131
hapmaprs863225131
1000 genomesrs863225131
hgdprs863225131
ensemblrs863225131
gopubmedrs863225131
geneviewrs863225131
scholarrs863225131
googlers863225131
pharmgkbrs863225131
gwascentralrs863225131
openSNPrs863225131
23andMers863225131
23andMe allrs863225131
SNP Nexus

SNPshotrs863225131
SNPdbers863225131
MSV3drs863225131
GWAS Ctlgrs863225131
Max Magnitude0
ClinVar
Risk rs863225131(G;G)
Alt rs863225131(G;G)
Reference rs863225131(T;T)
Significance Pathogenic
Disease Joubert syndrome 3
Variation info
Gene AHI1
CLNDBN Joubert syndrome 3
Reversed 1
HGVS NC_000006.11:g.135749895A>C
CLNSRC
CLNACC RCV000201542.1,