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Variant (rsID / SNP)

rs3742076

FOXM1

rs3742076 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXM1. Location: chromosome 12, position 2,968,169. The table records no clinical significance for this variant.

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Reference-table entries

FOXM1Not classified
Variant type
missense_variant
Chromosome / position
12:2968169
HGVS
NM_202002.3,c.2041T>C,p.Ser681Pro
Allele change
Silent

Associated conditions / phenotypes

Missense_S681P

Public references

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