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Variant (rsID / SNP)

rs4889241

PKD1L2

rs4889241 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKD1L2. Location: chromosome 16, position 81,157,324. The table records no clinical significance for this variant.

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Reference-table entries

PKD1L2Not classified
Variant type
missense_variant
Chromosome / position
16:81157324
HGVS
NM_001278425.2,c.4358C>T,p.Ser1453Phe
Allele change
Missense_P1454S

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.