Variant (rsID / SNP)
rs1559401
rs1559401 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKD1L3. Location: chromosome 16, position 72,011,181. The table records no clinical significance for this variant.
Reference-table entries
PKD1L3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 16:72011181
- HGVS
- NM_181536.2,c.1713C>A,p.His571Gln
- Allele change
- Missense_H571Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.