Variant (rsID / SNP)

rs2378757

rs2378757 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CTSL. Location: chromosome 9, position 90,343,780. The table records no clinical significance for this variant.

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Reference-table entries

CTSLNot classified

Variant type: intron_variant
Chromosome / position: 9:90343780
HGVS: NM_001257971.2,c.621+56A>C
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.