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rs386834008

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386834008(A;A)
Make rs386834008(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position59064355
GeneTRIM37
is asnp
is mentioned by
dbSNPrs386834008
ebirs386834008
HLIrs386834008
Exacrs386834008
Varsomers386834008
Maprs386834008
PheGenIrs386834008
hapmaprs386834008
1000 genomesrs386834008
hgdprs386834008
ensemblrs386834008
gopubmedrs386834008
geneviewrs386834008
scholarrs386834008
googlers386834008
pharmgkbrs386834008
gwascentralrs386834008
openSNPrs386834008
23andMers386834008
23andMe allrs386834008
SNP Nexus

SNPshotrs386834008
SNPdbers386834008
MSV3drs386834008
GWAS Ctlgrs386834008
Max Magnitude0
ClinVar
Risk rs386834008(A;A)
Alt rs386834008(A;A)
Reference rs386834008(G;G)
Significance Other
Disease Mulibrey nanism syndrome
Variation info
Gene TRIM37
CLNDBN Mulibrey nanism syndrome
Reversed 1
HGVS NC_000017.10:g.57141716C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005558.7,


[PMID 17100991] Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism.