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rs863225233

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225233(G;G)
Make rs863225233(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93815365
GeneTMEM67
is asnp
is mentioned by
dbSNPrs863225233
ebirs863225233
HLIrs863225233
Exacrs863225233
Varsomers863225233
Maprs863225233
PheGenIrs863225233
hapmaprs863225233
1000 genomesrs863225233
hgdprs863225233
ensemblrs863225233
gopubmedrs863225233
geneviewrs863225233
scholarrs863225233
googlers863225233
pharmgkbrs863225233
gwascentralrs863225233
openSNPrs863225233
23andMers863225233
23andMe allrs863225233
SNP Nexus

SNPshotrs863225233
SNPdbers863225233
MSV3drs863225233
GWAS Ctlgrs863225233
Max Magnitude0
ClinVar
Risk rs863225233(G;G)
Alt rs863225233(G;G)
Reference rs863225233(T;T)
Significance Pathogenic
Disease Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94827593T>G
CLNSRC
CLNACC RCV000201774.1,