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rs267607137

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607137(C;T)
Make rs267607137(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position140360131
GeneTRAPPC9
is asnp
is mentioned by
dbSNPrs267607137
ClinGenrs267607137
ebirs267607137
HLIrs267607137
Exacrs267607137
Varsomers267607137
Maprs267607137
PheGenIrs267607137
hapmaprs267607137
1000 genomesrs267607137
hgdprs267607137
ensemblrs267607137
gopubmedrs267607137
geneviewrs267607137
scholarrs267607137
googlers267607137
pharmgkbrs267607137
gwascentralrs267607137
openSNPrs267607137
23andMers267607137
23andMe allrs267607137
SNP Nexus

SNPshotrs267607137
SNPdbers267607137
MSV3drs267607137
GWAS Ctlgrs267607137
Max Magnitude0
ClinVar
Risk rs267607137(T;T)
Alt rs267607137(T;T)
Reference Rs267607137(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene TRAPPC9
CLNDBN Mental retardation, autosomal recessive 13
Reversed 1
HGVS NC_000008.10:g.141370230G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000795.2,