Variant (rsID / SNP)
rs915843
rs915843 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCG1. Location: chromosome 21, position 43,679,554. The table records no clinical significance for this variant.
Reference-table entries
ABCG1Not classified
- Variant type
- intron_variant
- Chromosome / position
- 21:43679554
- HGVS
- NM_004915.4,c.287-11626C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.