rs12069578

A SNP in the MFN2 gene on chromosome 1. Its most notable genotype is G;G: common in clinvar

Gene
MFN2
Location
Chr 112,004,010 (GRCh38)
Highest magnitude
0.0Typical
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon in clinvarTypical · 0.0100% of people

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

Frequency

Share of each genotype in 3 HapMap populations.

  • AverageG;G 100%
  • European ancestry (Utah)G;G 100%
  • Han Chinese (Beijing)G;G 100%
  • Japanese (Tokyo)G;G 100%

Other MFN2 SNPs

All MFN2 SNPs

Source and license

Adapted from rs12069578 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.