From: Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease
 | Fisher's Exact Test | McNemar's Test | Fisher's Exact Test | |||||
---|---|---|---|---|---|---|---|---|
Allele | Cases | Controls | p | Risk | p | Affected Mother | Affected Father | p |
1719A | 93.4% | 95.9% | 0.09 | - | 0.11 | 90.0% | 91.0% | 0.83 |
4580A | 97.2% | 97.4% | 0.84 | - | 1.00 | 95.0% | 98.5% | 0.24 |
7028C | 54.1% | 55.3% | 0.69 | - | 0.74 | 61.3% | 53.7% | 0.36 |
8251A | 94.9% | 95.1% | 0.88 | - | 1.00 | 87.5% | 95.5% | 0.09 |
9055A | 92.3% | 90.2% | 0.25 | + | 0.29 | 96.2% | 89.6% | 0.11 |
10398G | 19.4% | 20.9% | 0.57 | - | 0.62 | 20.0% | 20.9% | 0.89 |
10400T | 0.6% | 0.4% | 0.65 | + | 1.00 | 0.0% | 1.5% | 0.27 |
12308G | 21.4% | 23.3% | 0.48 | - | 0.52 | 21.2% | 23.9% | 0.70 |
13368A | 89.5% | 91.2% | 0.38 | - | 0.44 | 91.2% | 92.5% | 0.78 |
13708A | 88.0% | 86.8% | 0.55 | + | 0.61 | 86.2% | 91.0% | 0.37 |
16391A | 98.1% | 97.4% | 0.51 | + | 0.66 | 95.0% | 98.5% | 0.24 |
H | 43.6% | 42.9% | 0.84 | + | 0.90 | 36.2% | 46.3% | 0.22 |
I | 1.7% | 2.4% | 0.49 | - | 0.65 | 5.0% | 0.0% | 0.06 |
J | 9.2% | 10.9% | 0.38 | - | 0.43 | 12.5% | 7.5% | 0.31 |
K | 7.5% | 9.4% | 0.29 | - | 0.34 | 3.8% | 10.4% | 0.11 |
M | 0.6% | 0.4% | 0.65 | + | 1.00 | 0.0% | 1.5% | 0.27 |
T | 9.4% | 8.3% | 0.57 | + | 0.65 | 8.8% | 6.0% | 0.52 |
U | 12.6% | 13.0% | 0.84 | - | 0.92 | 17.5% | 10.4% | 0.22 |
V | 2.4% | 2.4% | 1.00 | - | 1.00 | 3.8% | 1.5% | 0.40 |
W | 1.7% | 1.7% | 1.00 | - | 1.00 | 3.8% | 1.5% | 0.40 |
X | 2.8% | 0.6% | 0.01 | + | 0.02 | 1.2% | 7.5% | 0.06 |
Other | 8.5% | 7.9% | 0.72 | + | 0.81 | 7.5% | 7.5% | 0.99 |
IJK vs. HMTUVWX | 18.4% | 22.6% | 0.11 | - | 0.12 | 21.2% | 17.9% | 0.61 |
JTUK vs. HIMVWX | 31.2% | 33.1% | 0.53 | - | 0.57 | 35.0% | 26.9% | 0.29 |
JTIWX vs. HKMUV | 24.8% | 23.9% | 0.76 | + | 0.82 | 31.2% | 22.4% | 0.23 |