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rs762543032

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs762543032(C;T)
Make rs762543032(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93755798
GeneTMEM67
is asnp
is mentioned by
dbSNPrs762543032
ebirs762543032
HLIrs762543032
Exacrs762543032
Varsomers762543032
Maprs762543032
PheGenIrs762543032
hapmaprs762543032
1000 genomesrs762543032
hgdprs762543032
ensemblrs762543032
gopubmedrs762543032
geneviewrs762543032
scholarrs762543032
googlers762543032
pharmgkbrs762543032
gwascentralrs762543032
openSNPrs762543032
23andMers762543032
23andMe allrs762543032
SNP Nexus

SNPshotrs762543032
SNPdbers762543032
MSV3drs762543032
GWAS Ctlgrs762543032
Max Magnitude0
ClinVar
Risk rs762543032(T;T)
Alt rs762543032(T;T)
Reference rs762543032(C;C)
Significance Pathogenic
Disease Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94768026C>T
CLNSRC
CLNACC RCV000201641.1,