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rs863225234

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225234(A;C)
Make rs863225234(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93808922
GeneTMEM67
is asnp
is mentioned by
dbSNPrs863225234
ebirs863225234
HLIrs863225234
Exacrs863225234
Varsomers863225234
Maprs863225234
PheGenIrs863225234
hapmaprs863225234
1000 genomesrs863225234
hgdprs863225234
ensemblrs863225234
gopubmedrs863225234
geneviewrs863225234
scholarrs863225234
googlers863225234
pharmgkbrs863225234
gwascentralrs863225234
openSNPrs863225234
23andMers863225234
23andMe allrs863225234
SNP Nexus

SNPshotrs863225234
SNPdbers863225234
MSV3drs863225234
GWAS Ctlgrs863225234
Max Magnitude0
ClinVar
Risk rs863225234(C;C)
Alt rs863225234(C;C)
Reference rs863225234(A;A)
Significance Pathogenic
Disease Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94821150A>C
CLNSRC
CLNACC RCV000201610.1,