Variant (rsID / SNP)
rs113259170
rs113259170 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMC3. Location: chromosome 9, position 133,948,176. Clinical significance in the table: Benign.
Reference-table entries
LAMC3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:133948176
- Cytoband
- 9q34.12
- HGVS
- NM_006059.4(LAMC3):c.3371C>T (p.Ser1124Phe)
- Allele change
- Missense_S1124F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.