Variant (rsID / SNP)

rs17860405

rs17860405 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CASP10. Location: chromosome 2, position 202,074,207. Clinical significance in the table: Benign.

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Reference-table entries

CASP10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:202074207
Cytoband: 2q33.1
HGVS: NM_032977.4(CASP10):c.1337A>G (p.Tyr446Cys)
Allele change: Missense_Y379C

Associated conditions / phenotypes

Autoimmune lymphoproliferative syndrome type 2A

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.