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

rs863225149

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225149(G;G)
Make rs863225149(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position93995879
GeneARL13B
is asnp
is mentioned by
dbSNPrs863225149
ebirs863225149
HLIrs863225149
Exacrs863225149
Varsomers863225149
Maprs863225149
PheGenIrs863225149
hapmaprs863225149
1000 genomesrs863225149
hgdprs863225149
ensemblrs863225149
gopubmedrs863225149
geneviewrs863225149
scholarrs863225149
googlers863225149
pharmgkbrs863225149
gwascentralrs863225149
openSNPrs863225149
23andMers863225149
23andMe allrs863225149
SNP Nexus

SNPshotrs863225149
SNPdbers863225149
MSV3drs863225149
GWAS Ctlgrs863225149
Max Magnitude0
ClinVar
Risk rs863225149(G;G)
Alt rs863225149(G;G)
Reference rs863225149(T;T)
Significance Pathogenic
Disease Joubert syndrome 8
Variation info
Gene ARL13B
CLNDBN Joubert syndrome 8
Reversed 0
HGVS NC_000003.11:g.93714723T>G
CLNSRC
CLNACC RCV000201642.1,