Variant (rsID / SNP)

rs9924371

rs9924371 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKD1L2. Location: chromosome 16, position 81,253,759. The table records no clinical significance for this variant.

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Reference-table entries

PKD1L2Not classified

Variant type: missense_variant
Chromosome / position: 16:81253759
HGVS: NM_001076780.2,c.217T>C,p.Trp73Arg
Allele change: Missense_W73R

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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