Variant (rsID / SNP)

rs16953240

rs16953240 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIERCE2, DNAAF4-CCPG1. Location: chromosome 15, position 55,700,981. The table records no clinical significance for this variant.

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Reference-table entries

PIERCE2Not classified

Variant type: missense_variant
Chromosome / position: 15:55700981
HGVS: NM_001198784.2,c.15C>A,p.Asn5Lys
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.