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Variant (rsID / SNP)

rs3191122

MKI67

rs3191122 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MKI67. Location: chromosome 10, position 129,900,858. The table records no clinical significance for this variant.

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Reference-table entries

MKI67Not classified
Variant type
synonymous_variant
Chromosome / position
10:129900858
HGVS
NM_002417.5,c.9246G>A,p.Ser3082Ser
Allele change
Synonymous_S2722S

Public references

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