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rs387907132

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387907132(A;G)
Make rs387907132(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position61366203
GeneTMEM138
is asnp
is mentioned by
dbSNPrs387907132
ebirs387907132
HLIrs387907132
Exacrs387907132
Varsomers387907132
Maprs387907132
PheGenIrs387907132
hapmaprs387907132
1000 genomesrs387907132
hgdprs387907132
ensemblrs387907132
gopubmedrs387907132
geneviewrs387907132
scholarrs387907132
googlers387907132
pharmgkbrs387907132
gwascentralrs387907132
openSNPrs387907132
23andMers387907132
23andMe allrs387907132
SNP Nexus

SNPshotrs387907132
SNPdbers387907132
MSV3drs387907132
GWAS Ctlgrs387907132
Max Magnitude0
ClinVar
Risk rs387907132(G;G)
Alt rs387907132(G;G)
Reference rs387907132(A;A)
Significance Pathogenic
Disease Joubert syndrome 16
Variation info
Gene TMEM138
CLNDBN Joubert syndrome 16
Reversed 0
HGVS NC_000011.9:g.61133675A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024187.2,