Variant (rsID / SNP)
rs707922
rs707922 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOM, BAG6. Location: chromosome 6, position 31,625,507. The table records no clinical significance for this variant.
Reference-table entries
APOMNot classified
- Variant type
- splice_region_variant&intron_variant
- Chromosome / position
- 6:31625507
- HGVS
- NM_019101.3,c.541+7G>T
- Allele change
- Silent
Associated conditions / phenotypes
Pulmonary Disease, Chronic Obstructive
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.