rs121912702
A SNP in the AGT gene on chromosome 1. Its most notable genotype is A;G: Carrier for a renal tubular dysgenesis mutation
- Gene
- AGT
- Location
- Chr 1230,710,247 (GRCh38)
- Highest magnitude
- 3.0Important
- Tested on
- Not on consumer chips
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- G;GGoodcommon in clinvar
- A;GMost notableBadCarrier for a renal tubular dysgenesis mutation
SNPedia records rs121912702 on the minus strand: (C;C), (C;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other AGT SNPs
- rs74315283C;TCarrier for a renal tubular dysgenesis mutationImportant
- rs387906578-;ACarrier for a renal tubular dysgenesis mutationImportant
- rs699G;Gincreased risk of hypertensionWorth knowing
- rs4762G;Gnormal riskTypical
- rs5050T;Tcommon in clinvarTypical
- rs5051C;Cnormal riskTypical
- rs7079G;Gcommon in clinvarTypical
- rs1926723T;Tcommon in clinvarTypical
Notes
From SNPedia
Notes
see OMIM 106150.0004
A;G
Unaffected in absence of a second AGT gene mutation
Source and license
Adapted from rs121912702 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.