Variant (rsID / SNP)

rs76835557

rs76835557 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMN1. Location: chromosome 15, position 33,091,084. Clinical significance in the table: Likely benign.

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Reference-table entries

FMN1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:33091084
Cytoband: 15q13.3
HGVS: NM_001277313.2(FMN1):c.4051G>A (p.Val1351Met)
Allele change: Missense_V1128M

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.