Variant (rsID / SNP)

rs35333794

rs35333794 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM2. Location: chromosome 4, position 154,216,548. Clinical significance in the table: Benign.

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Reference-table entries

TRIM2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:154216548
Cytoband: 4q31.3
HGVS: NM_015271.5(TRIM2):c.870C>T (p.Asn290=)
Allele change: Synonymous_N263N

Associated conditions / phenotypes

Charcot-Marie-Tooth disease type 2R

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.