Variant (rsID / SNP)

rs2305948

rs2305948 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KDR. Location: chromosome 4, position 55,979,558. The table records no clinical significance for this variant.

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Reference-table entries

KDRNot classified

Variant type: single nucleotide variant
Chromosome / position: 4:55979558
Cytoband: 4q12
HGVS: NM_002253.4(KDR):c.889G>A (p.Val297Ile)
Allele change: Missense_V297I

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.