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Variant (rsID / SNP)

rs147769257

FMN1

rs147769257 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMN1. Location: chromosome 15, position 33,096,488. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FMN1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
15:33096488
Cytoband
15q13.3
HGVS
NM_001277313.2(FMN1):c.3974A>G (p.Gln1325Arg)
Allele change
Missense_Q1102R

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.