Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs12451679

SLFN12L

rs12451679 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLFN12L. Location: chromosome 17, position 33,806,546. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

SLFN12LNot classified
Variant type
missense_variant
Chromosome / position
17:33806546
HGVS
NM_001363830.2,c.755C>T,p.Ser252Leu
Allele change
Missense_S257L

Public references

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