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rs267607136

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607136(C;T)
Make rs267607136(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position140397625
GeneTRAPPC9
is asnp
is mentioned by
dbSNPrs267607136
ebirs267607136
HLIrs267607136
Exacrs267607136
Varsomers267607136
Maprs267607136
PheGenIrs267607136
hapmaprs267607136
1000 genomesrs267607136
hgdprs267607136
ensemblrs267607136
gopubmedrs267607136
geneviewrs267607136
scholarrs267607136
googlers267607136
pharmgkbrs267607136
gwascentralrs267607136
openSNPrs267607136
23andMers267607136
23andMe allrs267607136
SNP Nexus

SNPshotrs267607136
SNPdbers267607136
MSV3drs267607136
GWAS Ctlgrs267607136
Max Magnitude0
ClinVar
Risk rs267607136(T;T)
Alt rs267607136(T;T)
Reference rs267607136(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene TRAPPC9
CLNDBN Mental retardation, autosomal recessive 13
Reversed 1
HGVS NC_000008.10:g.141407724G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000794.4,