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

rs863225229

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225229(A;G)
Make rs863225229(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93780608
GeneTMEM67
is asnp
is mentioned by
dbSNPrs863225229
ebirs863225229
HLIrs863225229
Exacrs863225229
Varsomers863225229
Maprs863225229
PheGenIrs863225229
hapmaprs863225229
1000 genomesrs863225229
hgdprs863225229
ensemblrs863225229
gopubmedrs863225229
geneviewrs863225229
scholarrs863225229
googlers863225229
pharmgkbrs863225229
gwascentralrs863225229
openSNPrs863225229
23andMers863225229
23andMe allrs863225229
SNP Nexus

SNPshotrs863225229
SNPdbers863225229
MSV3drs863225229
GWAS Ctlgrs863225229
Max Magnitude0
ClinVar
Risk rs863225229(G;G)
Alt rs863225229(G;G)
Reference rs863225229(A;A)
Significance Pathogenic
Disease Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94792836A>G
CLNSRC
CLNACC RCV000201733.1,