Variant (rsID / SNP)
rs1203892
rs1203892 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LINC00261. Location: chromosome 20, position 22,548,520. The table records no clinical significance for this variant.
Reference-table entries
LINC00261Not classified
- Variant type
- non_coding_transcript_exon_variant
- Chromosome / position
- 20:22548520
- HGVS
- NR_001558.3,n.137T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.