Table 6.

mtDNA variants shown to be associated with other diseases

*SNP	Basepair position	Minor Allele	**P-value
MitoT1005C	1005	C	0.50
MitoG1438A	1438	A	0.14
MitoA1555G	1555	G	0.12
MitoG3316A	3316	A	0.50
MitoA3796G	3796	G	0.25
MitoC4025T	4025	T	0.50
MitoC4171A	4171	A	0.50
MitoA4295G	4295	G	0.38
MitoC4640A	4640	A	0.49
MitoT5814C	5814	C	0.50
MitoC6489A	6489	A	0.25
MitoG7444A	7444	A	0.50
MitoA8348G	8348	G	0.50
MitoG9804A	9804	A	0.10
MitoT9957C	9957	C	0.50
MitoT10237C	10237	C	0.49
MitoA11084G	11084	G	0.50
MitoT11253C	11253	C	0.16
MitoG11696A	11696	A	0.51
MitoA12026G	12026	G	0.50
MitoT12297C	12297	C	0.50
MitoT12811C	12811	C	0.25
MitoA13637G	13637	G	0.02
MitoT14325C	14325	C	0.38
MitoG14831A	14831	A	0.25

^*Novel Phase 3 interrogated variation was compared against the “mtDNA Mutations with Reports of Disease-Association” from www.mitomap.org

^**Fisher’s exact test with 1 degree of freedom