rs6214

A SNP in the LOC105369942 gene on chromosome 12. Its most notable genotype is C;T: common in complete genomics

Gene
LOC105369942
Location
Chr 12102,399,791 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
45%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;TMost notableGoodcommon in complete genomicsTypical · 0.049% of people
  2. C;CGoodcommon in clinvarTypical · 0.030% of people

SNPedia records rs6214 on the minus strand: (A;G), (G;G). 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;T 49% C;C 30%
  • European ancestry (Utah)C;T 50% C;C 33%
  • Han Chinese (Beijing)C;T 53% C;C 24%
  • Japanese (Tokyo)C;T 50% C;C 24%
  • Yoruba (Nigeria)C;T 50% C;C 22%
  • African ancestry (Southwest US)C;T 47% C;C 30%
  • Chinese (Denver)C;T 65% C;C 14%
  • Gujarati IndianC;T 38% C;C 57%
  • Luhya (Kenya)C;T 54% C;C 23%
  • Mexican ancestry (Los Angeles)C;T 40% C;C 36%
  • Maasai (Kenya)C;T 51% C;C 30%
  • TuscanC;T 45% C;C 36%

Other LOC105369942 SNPs

All LOC105369942 SNPs

Source and license

Adapted from rs6214 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.