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Variant (rsID / SNP)

rs198977

KLK2

rs198977 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLK2. Location: chromosome 19, position 51,381,777. The table records no clinical significance for this variant.

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Reference-table entries

KLK2Not classified
Variant type
missense_variant
Chromosome / position
19:51381777
HGVS
NM_005551.5,c.748C>T,p.Arg250Trp
Allele change
Silent

Associated conditions / phenotypes

Prostate Cancer|Myopathy, Myosin Storage, Autosomal Recessive

Public references

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