Variant (rsID / SNP)

rs35618680

rs35618680 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCK2, NRL. Location: chromosome 14, position 24,572,812. Clinical significance in the table: Benign.

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Reference-table entries

PCK2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:24572812
Cytoband: 14q12
HGVS: NM_004563.4(PCK2):c.1562G>A (p.Arg521His)
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.