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rs863225230

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225230(A;A)
Make rs863225230(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93804807
GeneTMEM67
is asnp
is mentioned by
dbSNPrs863225230
ebirs863225230
HLIrs863225230
Exacrs863225230
Varsomers863225230
Maprs863225230
PheGenIrs863225230
hapmaprs863225230
1000 genomesrs863225230
hgdprs863225230
ensemblrs863225230
gopubmedrs863225230
geneviewrs863225230
scholarrs863225230
googlers863225230
pharmgkbrs863225230
gwascentralrs863225230
openSNPrs863225230
23andMers863225230
23andMe allrs863225230
SNP Nexus

SNPshotrs863225230
SNPdbers863225230
MSV3drs863225230
GWAS Ctlgrs863225230
Max Magnitude0
ClinVar
Risk rs863225230(A;A)
Alt rs863225230(A;A)
Reference rs863225230(C;C)
Significance Pathogenic
Disease Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94817035C>A
CLNSRC
CLNACC RCV000201638.1,