Variant (rsID / SNP)

rs2615542

rs2615542 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CENPE. Location: chromosome 4, position 104,066,461. The table records no clinical significance for this variant.

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Reference-table entries

CENPENot classified

Variant type: missense_variant
Chromosome / position: 4:104066461
HGVS: NM_001813.3,c.4603T>C,p.Phe1535Leu
Allele change: Missense_F1535L

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.