rs2070075(C;T)

Apparently benign variant

Magnitude
0.0Typical
Repute
Good
Frequency
3%Average of 4 populations
On SNPedia
rs2070075(C;T)
Gene
GALT

Frequency

Share of people with C;T in each HapMap population.

  • European ancestry (Utah)8%
  • Han Chinese (Beijing)2%
  • Japanese (Tokyo)0%
  • Yoruba (Nigeria)0%

Other genotypes of rs2070075

  1. C;CMost notableGoodcommon in complete genomicsTypical · 0.098% of people
  2. T;TGoodApparently benign variantTypical · 0.00% of people

All about rs2070075

Notes

From SNPedia

ClinVar currently indicates this variant is benign.

Source and license

Adapted from rs2070075(C;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.