Variant (rsID / SNP)

rs35636987

rs35636987 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KDR. Location: chromosome 4, position 55,981,531. Clinical significance in the table: Benign.

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Reference-table entries

KDRBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:55981531
Cytoband: 4q12
HGVS: NM_002253.4(KDR):c.406G>A (p.Val136Met)
Allele change: Missense_V136M

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.