Variant (rsID / SNP)

rs1064055

rs1064055 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYCBPAP, EPN3. Location: chromosome 17, position 48,608,717. The table records no clinical significance for this variant.

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Reference-table entries

MYCBPAPNot classified

Variant type: synonymous_variant
Chromosome / position: 17:48608717
HGVS: NM_001366294.2,c.2802T>C,p.Thr934Thr
Allele change: Synonymous_T961T

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.