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Variant (rsID / SNP)

rs964307

PKHD1L1

rs964307 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKHD1L1. Location: chromosome 8, position 110,413,762. The table records no clinical significance for this variant.

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Reference-table entries

PKHD1L1Not classified
Variant type
missense_variant
Chromosome / position
8:110413762
HGVS
NM_177531.6,c.1318T>C,p.Tyr440His
Allele change
Missense_Y440H

Public references

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