Variant (rsID / SNP)

rs307826

rs307826 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLT4. Location: chromosome 5, position 180,051,003. Clinical significance in the table: Benign.

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Reference-table entries

FLT4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:180051003
Cytoband: 5q35.3
HGVS: NM_182925.5(FLT4):c.1480A>G (p.Thr494Ala)
Allele change: Missense_T494A

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.