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Variant (rsID / SNP)

rs34255532

FLT4

rs34255532 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLT4. Location: chromosome 5, position 180,045,911. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FLT4Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
5:180045911
Cytoband
5q35.3
HGVS
NM_182925.5(FLT4):c.2860C>T (p.Pro954Ser)
Allele change
Missense_P954S

Associated conditions / phenotypes

Capillary infantile hemangioma|Carcinoma of colon

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.