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rs863225237

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225237(G;T)
Make rs863225237(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93782410
GeneTMEM67
is asnp
is mentioned by
dbSNPrs863225237
ebirs863225237
HLIrs863225237
Exacrs863225237
Varsomers863225237
Maprs863225237
PheGenIrs863225237
hapmaprs863225237
1000 genomesrs863225237
hgdprs863225237
ensemblrs863225237
gopubmedrs863225237
geneviewrs863225237
scholarrs863225237
googlers863225237
pharmgkbrs863225237
gwascentralrs863225237
openSNPrs863225237
23andMers863225237
23andMe allrs863225237
SNP Nexus

SNPshotrs863225237
SNPdbers863225237
MSV3drs863225237
GWAS Ctlgrs863225237
Max Magnitude0
ClinVar
Risk rs863225237(T;T)
Alt rs863225237(T;T)
Reference rs863225237(G;G)
Significance Pathogenic
Disease Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94794638G>T
CLNSRC
CLNACC RCV000201527.1,