rs16948048

A SNP in the ZNF652 gene on chromosome 17. Its most notable genotype is A;A: common/normal

Gene
ZNF652
Location
Chr 1749,363,104 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
31%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon/normalTypical · 0.052% of people

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

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageA;A 52%
  • European ancestry (Utah)A;A 34%
  • Han Chinese (Beijing)A;A 67%
  • Japanese (Tokyo)A;A 79%
  • Yoruba (Nigeria)A;A 34%
  • African ancestry (Southwest US)A;A 39%
  • Chinese (Denver)A;A 61%
  • Gujarati IndianA;A 70%
  • Luhya (Kenya)A;A 41%
  • Mexican ancestry (Los Angeles)A;A 50%
  • Maasai (Kenya)A;A 49%
  • TuscanA;A 50%

Conditions, medicines and genes

Other ZNF652 SNPs

All ZNF652 SNPs

Notes

From SNPedia

Notes

23andMe blog blood pressure Confirmation of top polymorphisms in hypertension genome wide association study among Han Chinese.

Source and license

Adapted from rs16948048 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.