Variant (rsID / SNP)

rs2307313

rs2307313 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MCM2. Location: chromosome 3, position 127,338,035. Clinical significance in the table: Benign.

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Reference-table entries

MCM2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:127338035
Cytoband: 3q21.3
HGVS: NM_004526.4(MCM2):c.2179G>A (p.Ala727Thr)
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.