Variant (rsID / SNP)
rs1678339
rs1678339 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCC4. Location: chromosome 13, position 95,727,780. The table records no clinical significance for this variant.
Reference-table entries
ABCC4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 13:95727780
- HGVS
- NM_005845.5,c.2712A>G,p.Leu904Leu
- Allele change
- Synonymous_L904L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.