Variant (rsID / SNP)
rs144873879
rs144873879 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SH3TC2. Location: chromosome 5, position 148,384,346. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
SH3TC2Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:148384346
- Cytoband
- 5q32
- HGVS
- NM_024577.4(SH3TC2):c.3795G>C (p.Leu1265=)
- Allele change
- Synonymous_L1265L
Associated conditions / phenotypes
Susceptibility to mononeuropathy of the median nerve, mild|Charcot-Marie-Tooth disease type 4|Charcot-Marie-Tooth disease type 4C|Charcot-Marie-Tooth disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.