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rs863225225

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225225(A;A)
Make rs863225225(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93797184
GeneTMEM67
is asnp
is mentioned by
dbSNPrs863225225
ebirs863225225
HLIrs863225225
Exacrs863225225
Varsomers863225225
Maprs863225225
PheGenIrs863225225
hapmaprs863225225
1000 genomesrs863225225
hgdprs863225225
ensemblrs863225225
gopubmedrs863225225
geneviewrs863225225
scholarrs863225225
googlers863225225
pharmgkbrs863225225
gwascentralrs863225225
openSNPrs863225225
23andMers863225225
23andMe allrs863225225
SNP Nexus

SNPshotrs863225225
SNPdbers863225225
MSV3drs863225225
GWAS Ctlgrs863225225
Max Magnitude0
ClinVar
Risk rs863225225(A;A)
Alt rs863225225(A;A)
Reference rs863225225(C;C)
Significance Pathogenic
Disease Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94809412C>A
CLNSRC
CLNACC RCV000201665.1,