Variant (rsID / SNP)

rs1797517

rs1797517 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLRF2, CLEC2A. Location: chromosome 12, position 10,041,364. The table records no clinical significance for this variant.

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Reference-table entries

KLRF2Not classified

Variant type: missense_variant
Chromosome / position: 12:10041364
HGVS: NM_001190765.1,c.202G>A,p.Val68Ile
Allele change: Missense_V68I

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.