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rs863225240

From SNPedia

Orientationplus
Make rs863225240(-;-)
Make rs863225240(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93803689
GeneTMEM67
is asnp
is mentioned by
dbSNPrs863225240
ClinGenrs863225240
ebirs863225240
HLIrs863225240
Exacrs863225240
Varsomers863225240
Maprs863225240
PheGenIrs863225240
hapmaprs863225240
1000 genomesrs863225240
hgdprs863225240
ensemblrs863225240
gopubmedrs863225240
geneviewrs863225240
scholarrs863225240
googlers863225240
pharmgkbrs863225240
gwascentralrs863225240
openSNPrs863225240
23andMers863225240
23andMe allrs863225240
SNP Nexus

SNPshotrs863225240
SNPdbers863225240
MSV3drs863225240
GWAS Ctlgrs863225240
Max Magnitude
ClinVar
Risk
Alt
Reference Rs863225240(G;G)
Significance Probable-Pathogenic
Disease Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94815917delG
CLNSRC
CLNACC RCV000201630.1,