rs199476102

A SNP in the MIR1225 gene on chromosome 16. Its most notable genotype is C;T: Polycystic Kidney Disease (predicted)

Gene
MIR1225
Location
Chr 162,090,309 (GRCh38)
Highest magnitude
5.0Very important
Tested on
AncestryDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;TMost notableBadPolycystic Kidney Disease (predicted)Very important · 5.0
  2. C;CGoodcommon in clinvarTypical · 0.0

SNPedia records rs199476102 on the minus strand: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Conditions, medicines and genes

Other MIR1225 SNPs

All MIR1225 SNPs

Notes

From SNPedia

Notes

Polycystic Kidney disease; see OMIM 601313.0015 NM_001009944.2:c.12420G>A The variant allele of this SNP is considered either "definitely pathogenic" or "highly likely pathogenic" for autosomal dominant polycystic kidney disease in the PKD Foundation database.

Source and license

Adapted from rs199476102 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.