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rs863225235

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225235(A;A)
Make rs863225235(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93782444
GeneTMEM67
is asnp
is mentioned by
dbSNPrs863225235
dbSNP (old)rs863225235
ClinGenrs863225235
ebirs863225235
HLIrs863225235
Exacrs863225235
Gnomadrs863225235
Varsomers863225235
Maprs863225235
PheGenIrs863225235
Biobankrs863225235
1000 genomesrs863225235
hgdprs863225235
ensemblrs863225235
gopubmedrs863225235
geneviewrs863225235
scholarrs863225235
googlers863225235
pharmgkbrs863225235
gwascentralrs863225235
openSNPrs863225235
23andMers863225235
23andMe allrs863225235
SNP Nexus

SNPshotrs863225235
SNPdbers863225235
MSV3drs863225235
GWAS Ctlgrs863225235
Max Magnitude0
ClinVar
Risk rs863225235(A;A)
Alt rs863225235(A;A)
Reference Rs863225235(C;C)
Significance Pathogenic
Disease Joubert syndrome 6 not provided
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6 not provided
Reversed 0
HGVS NC_000008.10:g.94794672C>A
CLNSRC UniProtKB (protein)
CLNACC RCV000201528.1, RCV000419395.1,