Variant (rsID / SNP)

rs121917811

rs121917811 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGTR2. Clinical significance in the table: Uncertain significance.

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Reference-table entries

AGTR2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Cytoband: Xq23
HGVS: NM_000686.5(AGTR2):c.1009A>G (p.Ile337Val)
Allele change: Missense_I337V

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.