The G (minor) allele is associated with:

  • Disrupted binding site to STAT1 and diminishes IFNy protein,
  • This will cause an inability to combat viral infections.

rs10757278

Parent Gene: CDKN2B-AS1, DMRTA1, STAT1

Importance: 3
Less common allele: G = 41%
More common allele: A = 59%
My Genotype: Log In
Risk Allele: G

Disease/Trait: Myocardial Infarction

The G allele of rs10757278 is reported to be associated with Myocardial Infarction (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Myocardial infarction.