rs28383481

A SNP in the SLC22A5 gene on chromosome 5. Its most notable genotype is G;G: common in clinvar

Gene
SLC22A5
Location
Chr 5132,393,688 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
<1%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in clinvarTypical · 0.098% of people

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

Frequency

Share of each genotype in one HapMap population.

  • TuscanG;G 98%

Other SLC22A5 SNPs

All SLC22A5 SNPs

Notes

From SNPedia

Notes

minor allele should be reclassified as benign according to

Source and license

Adapted from rs28383481 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.