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Variant (rsID / SNP)

rs17358402

PKD1L3

rs17358402 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKD1L3. Location: chromosome 16, position 71,967,927. The table records no clinical significance for this variant.

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Reference-table entries

PKD1L3Not classified
Variant type
missense_variant
Chromosome / position
16:71967927
HGVS
NM_181536.2,c.4709G>A,p.Arg1570His
Allele change
Missense_V1571I

Public references

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