Variant (rsID / SNP)
rs569511
rs569511 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKD2L1. Location: chromosome 10, position 102,089,663. The table records no clinical significance for this variant.
Reference-table entries
PKD2L1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:102089663
- HGVS
- NM_001253837.2,c.35G>A,p.Cys12Tyr
- Allele change
- Missense_C12Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.