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Variant (rsID / SNP)

rs2586514

SLFN12

rs2586514 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLFN12. Location: chromosome 17, position 33,749,546. The table records no clinical significance for this variant.

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Reference-table entries

SLFN12Not classified
Variant type
missense_variant
Chromosome / position
17:33749546
HGVS
NM_001289009.2,c.502T>C,p.Cys168Arg
Allele change
Missense_C168R

Public references

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