Variant (rsID / SNP)
rs12121707
rs12121707 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SELENON. Location: chromosome 1, position 26,126,680. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
SELENONConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:26126680
- Cytoband
- 1p36.11
- HGVS
- NM_020451.2(SELENON):c.-42T>C
- Allele change
- Silent
Associated conditions / phenotypes
SEPN1-Related Disorders
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.