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Variant (rsID / SNP)

rs9935113

PKD1L2

rs9935113 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKD1L2. Location: chromosome 16, position 81,211,496. The table records no clinical significance for this variant.

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Reference-table entries

PKD1L2Not classified
Variant type
missense_variant
Chromosome / position
16:81211496
HGVS
NM_001278425.2,c.298G>T,p.Gly100Cys
Allele change
Missense_G100C

Public references

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