Variant (rsID / SNP)

rs181961770

rs181961770 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FSCN2. Location: chromosome 17, position 79,496,003. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FSCN2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 17:79496003
Cytoband: 17q25.3
HGVS: NM_012418.4(FSCN2):c.446G>A (p.Arg149Gln)
Allele change: Missense_R149Q

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.