Variant (rsID / SNP)

rs3745535

rs3745535 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLK10. Location: chromosome 19, position 51,520,487. The table records no clinical significance for this variant.

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Reference-table entries

KLK10Not classified

Variant type: missense_variant
Chromosome / position: 19:51520487
HGVS: NM_001077500.2,c.148T>G,p.Ser50Ala
Allele change: Missense_S50A

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.