rs3218713(C;T)

Familial Hypertrophic Cardiomyopathy

Magnitude
6.0Very important
Repute
Bad
Frequency
0%Average of 4 populations
On SNPedia
rs3218713(A;G)Minus strand
Gene
MYH7

Frequency

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

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

Other genotypes of rs3218713

  1. T;TBadFamilial Hypertrophic CardiomyopathyVery important · 6.00% of people
  2. C;CGoodcommon in clinvarTypical · 0.0100% of people
  3. A;CMost notableBadFamilial Hypertrophic CardiomyopathyVery important · 6.20% of people

All about rs3218713

Notes

From SNPedia

Familial hypertrophic cardiomyopathy see also OMIM 160760.0002

Source and license

Adapted from rs3218713(A;G) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.