Variant (rsID / SNP)
rs41265137
rs41265137 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN3A. Location: chromosome 2, position 165,947,079. Clinical significance in the table: Benign.
Reference-table entries
SCN3ABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:165947079
- Cytoband
- 2q24.3
- HGVS
- NM_006922.4(SCN3A):c.5584G>T (p.Gly1862Cys)
- Allele change
- Missense_G1813C
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.