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rs863225224

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225224(A;G)
Make rs863225224(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93793299
GeneTMEM67
is asnp
is mentioned by
dbSNPrs863225224
ebirs863225224
HLIrs863225224
Exacrs863225224
Varsomers863225224
Maprs863225224
PheGenIrs863225224
hapmaprs863225224
1000 genomesrs863225224
hgdprs863225224
ensemblrs863225224
gopubmedrs863225224
geneviewrs863225224
scholarrs863225224
googlers863225224
pharmgkbrs863225224
gwascentralrs863225224
openSNPrs863225224
23andMers863225224
23andMe allrs863225224
SNP Nexus

SNPshotrs863225224
SNPdbers863225224
MSV3drs863225224
GWAS Ctlgrs863225224
Max Magnitude0
ClinVar
Risk rs863225224(G;G)
Alt rs863225224(G;G)
Reference rs863225224(A;A)
Significance Pathogenic
Disease Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94805527A>G
CLNSRC
CLNACC RCV000201579.1,