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Variant (rsID / SNP)

rs3816281

PLEK

rs3816281 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLEK. Location: chromosome 2, position 68,607,947. The table records no clinical significance for this variant.

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Reference-table entries

PLEKNot classified
Variant type
missense_variant
Chromosome / position
2:68607947
HGVS
NM_002664.3,c.291G>T,p.Lys97Asn
Allele change
Missense_K97N

Associated conditions / phenotypes

Graft-Versus-Host Disease|Acute Graft Versus Host Disease

Public references

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