Variant (rsID / SNP)

rs307821

rs307821 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLT4. Location: chromosome 5, position 180,030,313. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FLT4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:180030313
Cytoband: 5q35.3
HGVS: NM_182925.5(FLT4):c.3971G>T (p.Arg1324Leu)
Allele change: Missense_R1324L

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.