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Variant (rsID / SNP)

rs35960726

HAVCR2

rs35960726 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HAVCR2. Location: chromosome 5, position 156,533,741. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

HAVCR2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
5:156533741
Cytoband
5q33.3
HGVS
NM_032782.5(HAVCR2):c.291A>G (p.Ile97Met)
Allele change
Missense_I97M

Associated conditions / phenotypes

Subcutaneous panniculitis-like T-cell lymphoma

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.