Variant (rsID / SNP)

rs114171764

rs114171764 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PALLD. Location: chromosome 4, position 169,837,051. Clinical significance in the table: Likely benign.

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Reference-table entries

PALLDLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:169837051
Cytoband: 4q32.3
HGVS: NM_001166108.2(PALLD):c.2723G>A (p.Arg908His)
Allele change: Missense_R908H

Associated conditions / phenotypes

Pancreatic adenocarcinoma

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.