Variant (rsID / SNP)
rs1040285
rs1040285 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC162P. Location: chromosome 6, position 109,583,186. The table records no clinical significance for this variant.
Reference-table entries
CCDC162PNot classified
- Variant type
- non_coding_transcript_exon_variant
- Chromosome / position
- 6:109583186
- HGVS
- NR_152435.1,n.2863A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.