Variant (rsID / SNP)

rs144284959

rs144284959 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCK2, NRL. Location: chromosome 14, position 24,572,929. Clinical significance in the table: Uncertain significance.

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Reference-table entries

PCK2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 14:24572929
Cytoband: 14q12
HGVS: NM_004563.4(PCK2):c.1679G>A (p.Arg560Gln)
Allele change: Silent

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.