Variant (rsID / SNP)

rs4762

rs4762 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGT. Location: chromosome 1, position 230,845,977. 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: 1:230845977
Cytoband: 1q42.2
HGVS: NM_000029.4(AGT):c.620C>T (p.Thr207Met)
Allele change: Missense_T207M

Associated conditions / phenotypes

Renal tubular dysgenesis

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.