rs17235416

A SNP in the SLC11A1 gene on chromosome 2. Its most notable genotype is I;I: common genotype

Gene
SLC11A1
Location
Chr 2218,395,091 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
10%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. I;IMost notableGoodcommon genotypeTypical · 0.0
  2. TGTG;TGTGGoodcommon/normalTypical · 0.0

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

Other SLC11A1 SNPs

All SLC11A1 SNPs

Notes

From SNPedia

Notes

no association with tuberculosis Sex- and age-dependent association of SLC11A1 polymorphisms with tuberculosis in Chinese: a case control study. NRAMP1 (SLC11A1) gene polymorphisms that correlate with autoimmune versus infectious disease susceptibility in tuberculosis and rheumatoid arthritis. CXCR1 and SLC11A1 polymorphisms affect susceptibility to cutaneous leishmaniasis in Brazil: a case-control and family-based study. Polymorphisms in IL-1beta, vitamin D receptor Fok1, and Toll-like receptor 2 are associated with extrapulmonary tuberculosis. SLC11A1 (NRAMP1) polymorphisms and tuberculosis susceptibility: updated systematic review and meta-analysis.

Source and license

Adapted from rs17235416 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.