Variant (rsID / SNP)

rs146874723

rs146874723 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMN2. Location: chromosome 1, position 240,370,769. Clinical significance in the table: Likely benign.

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Reference-table entries

FMN2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:240370769
Cytoband: 1q43
HGVS: NM_020066.5(FMN2):c.2657T>G (p.Met886Arg)
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.