Variant (rsID / SNP)

rs149745504

rs149745504 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KDR. Location: chromosome 4, position 55,964,925. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

KDRLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:55964925
Cytoband: 4q12
HGVS: NM_002253.4(KDR):c.2312C>T (p.Thr771Met)
Allele change: Missense_T771M

Associated conditions / phenotypes

High myopia|Tufted angioma of skin

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.