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rs863225228

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225228(C;T)
Make rs863225228(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93787884
GeneTMEM67
is asnp
is mentioned by
dbSNPrs863225228
ebirs863225228
HLIrs863225228
Exacrs863225228
Varsomers863225228
Maprs863225228
PheGenIrs863225228
hapmaprs863225228
1000 genomesrs863225228
hgdprs863225228
ensemblrs863225228
gopubmedrs863225228
geneviewrs863225228
scholarrs863225228
googlers863225228
pharmgkbrs863225228
gwascentralrs863225228
openSNPrs863225228
23andMers863225228
23andMe allrs863225228
SNP Nexus

SNPshotrs863225228
SNPdbers863225228
MSV3drs863225228
GWAS Ctlgrs863225228
Max Magnitude0
ClinVar
Risk rs863225228(T;T)
Alt rs863225228(T;T)
Reference rs863225228(C;C)
Significance Pathogenic
Disease Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94800112C>T
CLNSRC
CLNACC RCV000201544.1,