rs6426748

A SNP on chromosome 1. Its most notable genotype is C;C: common in complete genomics

Gene
None listed
Location
Chr 122,381,072 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
19%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in complete genomicsTypical · 0.065% of people

On SNPedia: (C;C). 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.

  • AverageC;C 65%
  • European ancestry (Utah)C;C 72%
  • Han Chinese (Beijing)C;C 56%
  • Japanese (Tokyo)C;C 61%
  • Yoruba (Nigeria)C;C 43%
  • African ancestry (Southwest US)C;C 63%
  • Chinese (Denver)C;C 65%
  • Gujarati IndianC;C 79%
  • Luhya (Kenya)C;C 52%
  • Mexican ancestry (Los Angeles)C;C 91%
  • Maasai (Kenya)C;C 49%
  • TuscanC;C 80%

Notes

From SNPedia

Notes

rs6426748 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone mineral density variations, lower for carriers of the C allele rs6426748 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteoporotic fractures 1.15 times for carriers of the C allele

Source and license

Adapted from rs6426748 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.