Modeling of mitochondrial genetic polymorphisms reveals induction of heteroplasmy by pleiotropic disease locus 10398A>G.

Of the 764 SNPs, 98 of them were nominally significant from our data using a threshold of P < 0.01, whereas one would expect only 7.64 to be significant under the null hypothesis ( P = 7.4 × 10 –74 ).

also in 807 other papers