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rs386834009

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386834009(G;T)
Make rs386834009(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position59061086
GeneTRIM37
is asnp
is mentioned by
dbSNPrs386834009
ebirs386834009
HLIrs386834009
Exacrs386834009
Varsomers386834009
Maprs386834009
PheGenIrs386834009
hapmaprs386834009
1000 genomesrs386834009
hgdprs386834009
ensemblrs386834009
gopubmedrs386834009
geneviewrs386834009
scholarrs386834009
googlers386834009
pharmgkbrs386834009
gwascentralrs386834009
openSNPrs386834009
23andMers386834009
23andMe allrs386834009
SNP Nexus

SNPshotrs386834009
SNPdbers386834009
MSV3drs386834009
GWAS Ctlgrs386834009
Max Magnitude0
ClinVar
Risk rs386834009(T;T)
Alt rs386834009(T;T)
Reference rs386834009(G;G)
Significance Probable-Pathogenic
Disease Mulibrey nanism syndrome
Variation info
Gene TRIM37
CLNDBN Mulibrey nanism syndrome
Reversed 1
HGVS NC_000017.10:g.57138447C>A
CLNSRC ClinVar
CLNACC RCV000049987.1,


[PMID 15108285] Novel mutations in the TRIM37 gene in Mulibrey Nanism.