Variant (rsID / SNP)

rs2232548

rs2232548 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLRF1. Location: chromosome 12, position 9,985,915. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

KLRF1Not classified

Variant type: missense_variant
Chromosome / position: 12:9985915
HGVS: NM_016523.3,c.201G>T,p.Leu67Phe
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.