rs193008

A SNP in the SLC44A1 gene on chromosome 9. Its most notable genotype is T;T: common in complete genomics

Gene
SLC44A1
Location
Chr 9105,280,525 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
23%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in complete genomicsTypical · 0.064% of people

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

Frequency

Share of each genotype in 5 HapMap populations.

  • AverageT;T 64%
  • European ancestry (Utah)T;T 86%
  • Han Chinese (Beijing)T;T 73%
  • Japanese (Tokyo)T;T 84%
  • Yoruba (Nigeria)T;T 10%
  • Mexican ancestry (Los Angeles)T;T 70%

Conditions, medicines and genes

Notes

From SNPedia

Notes

635 lung cancer cases with onset of disease below 51 years of age and 1,300 controls. major alleles associated with increased in risk of early-onset lung cancer modified by smoking. *rs1938901 (P = 0.0089) *rs193008 (P = 0.0108) *rs996999 (P = 0.0459). For rs996999, significance vanished after correction for multiple testing. odds ratio between 1.2 and 1.3 (95% confidence interval, 1.0-1.5)

Source and license

Adapted from rs193008 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.