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rs587780486

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780486(G;T)
Make rs587780486(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position140451007
GeneTRAPPC9
is asnp
is mentioned by
dbSNPrs587780486
ebirs587780486
HLIrs587780486
Exacrs587780486
Varsomers587780486
Maprs587780486
PheGenIrs587780486
hapmaprs587780486
1000 genomesrs587780486
hgdprs587780486
ensemblrs587780486
gopubmedrs587780486
geneviewrs587780486
scholarrs587780486
googlers587780486
pharmgkbrs587780486
gwascentralrs587780486
openSNPrs587780486
23andMers587780486
23andMe allrs587780486
SNP Nexus

SNPshotrs587780486
SNPdbers587780486
MSV3drs587780486
GWAS Ctlgrs587780486
Max Magnitude0
ClinVar
Risk rs587780486(T;T)
Alt rs587780486(T;T)
Reference rs587780486(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene TRAPPC9
CLNDBN Mental retardation, autosomal recessive 13
Reversed 1
HGVS NC_000008.10:g.141461106C>A
CLNSRC
CLNACC RCV000118683.1,