Variant (rsID / SNP)

rs147827860

rs147827860 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HAVCR2. Location: chromosome 5, position 156,533,730. Clinical significance in the table: Benign.

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Reference-table entries

HAVCR2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:156533730
Cytoband: 5q33.3
HGVS: NM_032782.5(HAVCR2):c.302C>T (p.Thr101Ile)
Allele change: Missense_T101I

Associated conditions / phenotypes

Subcutaneous panniculitis-like T-cell lymphoma

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.