Variant (rsID / SNP)

rs1063535

rs1063535 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MKI67. Location: chromosome 10, position 129,902,281. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MKI67Not classified

Variant type: missense_variant
Chromosome / position: 10:129902281
HGVS: NM_002417.5,c.7823C>T,p.Pro2608Leu
Allele change: Missense_P2248L

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.