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rs863225231

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225231(C;G)
Make rs863225231(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93782455
GeneTMEM67
is asnp
is mentioned by
dbSNPrs863225231
ebirs863225231
HLIrs863225231
Exacrs863225231
Varsomers863225231
Maprs863225231
PheGenIrs863225231
hapmaprs863225231
1000 genomesrs863225231
hgdprs863225231
ensemblrs863225231
gopubmedrs863225231
geneviewrs863225231
scholarrs863225231
googlers863225231
pharmgkbrs863225231
gwascentralrs863225231
openSNPrs863225231
23andMers863225231
23andMe allrs863225231
SNP Nexus

SNPshotrs863225231
SNPdbers863225231
MSV3drs863225231
GWAS Ctlgrs863225231
Max Magnitude0
ClinVar
Risk rs863225231(G;G)
Alt rs863225231(G;G)
Reference rs863225231(C;C)
Significance Pathogenic
Disease Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94794683C>G
CLNSRC
CLNACC RCV000201732.1,