Variant (rsID / SNP)

rs2010963

rs2010963 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VEGFA. Location: chromosome 6, position 43,738,350. Clinical significance in the table: Benign.

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Reference-table entries

VEGFABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:43738350
Cytoband: 6p21.1
HGVS: NM_003376.6(VEGFA):c.-94C>G
Allele change: Silent

Associated conditions / phenotypes

Microvascular complications of diabetes, susceptibility to, 1

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.