Variant (rsID / SNP)

rs186367879

rs186367879 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FSCN2. Location: chromosome 17, position 79,502,218. Clinical significance in the table: Benign.

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Reference-table entries

FSCN2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:79502218
Cytoband: 17q25.3
HGVS: NM_012418.4(FSCN2):c.967G>A (p.Ala323Thr)
Allele change: Missense_A323T

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.