Variant (rsID / SNP)

rs2071498

rs2071498 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MKI67. Location: chromosome 10, position 129,917,560. The table records no clinical significance for this variant.

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Reference-table entries

MKI67Not classified

Variant type: missense_variant
Chromosome / position: 10:129917560
HGVS: NM_002417.5,c.311A>G,p.Asn104Ser
Allele change: Missense_N104S

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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