rs121918239

A SNP in the SLC34A3 gene on chromosome 9. Its most notable genotype is A;G: Carrier of a mutation for hypophosphatemic rickets with hypercalciuria

Gene
SLC34A3
Location
Chr 9137,233,404 (GRCh38)
Highest magnitude
3.0Important
Tested on
AncestryDNA
Minor allele frequency
<1%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;GMost notableBadCarrier of a mutation for hypophosphatemic rickets with hypercalciuriaImportant · 3.0
  2. G;GGoodcommon in clinvarTypical · 0.0

On SNPedia: (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Other SLC34A3 SNPs

All SLC34A3 SNPs

Notes

From SNPedia

Notes

rs121918239, also known as c.756G>A, is a relatively rare mutation in the SLC34A3 gene on chromosome 9. The rs121918239(A) mutation is considered pathogenic for hypophosphatemic rickets with hypercalciuria, a recessively inherited condition.

A;G

Unaffected in absence of another pathogenic mutation in the SLC34A3 gene

Source and license

Adapted from rs121918239 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.