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Variant (rsID / SNP)

rs114946738

PALLD

rs114946738 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PALLD. Location: chromosome 4, position 169,433,386. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

PALLDConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
4:169433386
Cytoband
4q32.3
HGVS
NM_001166108.2(PALLD):c.731A>G (p.Gln244Arg)
Allele change
Missense_Q244R

Associated conditions / phenotypes

Pancreatic cancer, susceptibility to, 1

Public references

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