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Variant (rsID / SNP)

rs1060463

CYP4F11

rs1060463 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP4F11. Location: chromosome 19, position 16,025,176. The table records no clinical significance for this variant.

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Reference-table entries

CYP4F11Not classified
Variant type
missense_variant
Chromosome / position
19:16025176
HGVS
NM_001128932.2,c.1336G>A,p.Asp446Asn
Allele change
Missense_D446N

Associated conditions / phenotypes

Lung Cancer

Public references

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