Variant (rsID / SNP)

rs13087457

rs13087457 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MCM2. Location: chromosome 3, position 127,334,777. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MCM2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:127334777
Cytoband: 3q21.3
HGVS: NM_004526.4(MCM2):c.1501G>A (p.Gly501Arg)
Allele change: Silent

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.