Variant (rsID / SNP)

rs2301826

rs2301826 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRC1. Location: chromosome 15, position 91,525,197. Clinical significance in the table: Uncertain significance.

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Reference-table entries

PRC1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 15:91525197
Cytoband: 15q26.1
HGVS: NM_003981.4(PRC1):c.282G>A (p.Thr94=)
Allele change: Synonymous_T94T

Associated conditions / phenotypes

Familial cancer of breast

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.