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rs387907134

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907134(A;A)
Make rs387907134(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position61367998
GeneTMEM138
is asnp
is mentioned by
dbSNPrs387907134
ebirs387907134
HLIrs387907134
Exacrs387907134
Varsomers387907134
Maprs387907134
PheGenIrs387907134
hapmaprs387907134
1000 genomesrs387907134
hgdprs387907134
ensemblrs387907134
gopubmedrs387907134
geneviewrs387907134
scholarrs387907134
googlers387907134
pharmgkbrs387907134
gwascentralrs387907134
openSNPrs387907134
23andMers387907134
23andMe allrs387907134
SNP Nexus

SNPshotrs387907134
SNPdbers387907134
MSV3drs387907134
GWAS Ctlgrs387907134
Max Magnitude0
ClinVar
Risk rs387907134(A;A)
Alt rs387907134(A;A)
Reference rs387907134(G;G)
Significance Pathogenic
Disease Joubert syndrome 16
Variation info
Gene TMEM138
CLNDBN Joubert syndrome 16
Reversed 0
HGVS NC_000011.9:g.61135470G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000024189.2,