Variant (rsID / SNP)

rs699

rs699 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGT. Location: chromosome 1, position 230,845,794. Clinical significance in the table: Benign.

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Reference-table entries

AGTBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:230845794
Cytoband: 1q42.2
HGVS: NM_000029.4(AGT):c.803T>C (p.Met268Thr)
Allele change: Missense_M268T

Associated conditions / phenotypes

Preeclampsia, susceptibility to|Susceptibility to progression to renal failure in IgA nephropathy|Hypertension, essential, susceptibility to|Renal tubular dysgenesis|Hypertensive disorder

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.