Variant (rsID / SNP)

rs12946

rs12946 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLK3. Location: chromosome 19, position 51,361,315. The table records no clinical significance for this variant.

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Reference-table entries

KLK3Not classified

Variant type: synonymous_variant
Chromosome / position: 19:51361315
HGVS: NM_001648.2,c.237C>T,p.Ser79Ser
Allele change: Synonymous_S79S

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.