Variant (rsID / SNP)

rs3747835

rs3747835 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM32. Location: chromosome 9, position 119,461,243. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TRIM32Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 9:119461243
Cytoband: 9q33.1
HGVS: NM_012210.4(TRIM32):c.1222C>T (p.Arg408Cys)
Allele change: Silent

Associated conditions / phenotypes

Bardet-Biedl syndrome 11|Bardet-Biedl syndrome|Sarcotubular myopathy

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.