Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113994095
POLG ; MIR6766
0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 21
rs267606959
POLG
0.732 0.200 15 89318986 missense variant G/A snv 2.0E-05 15
rs113994098
POLG
0.742 0.320 15 89321792 missense variant C/T snv 1.5E-04 2.7E-04 9
rs113994096
POLG
0.827 0.080 15 89325639 missense variant G/A snv 1.5E-03 1.6E-03 7
rs121918054
POLG
0.807 0.240 15 89323460 missense variant C/G;T snv 6.9E-04; 4.0E-06 7
rs113994094
POLG
0.827 0.080 15 89330184 missense variant G/A snv 1.5E-03 1.6E-03 6
rs121918044
POLG
0.807 0.240 15 89329055 missense variant A/C snv 5.7E-05 3.5E-05 6
rs144500145
POLG
0.807 0.240 15 89321780 missense variant G/A snv 4.8E-05 6.3E-05 6
rs201732356
POLG
0.807 0.240 15 89318737 missense variant G/A;C snv 8.0E-06 6
rs201477273
POLG
0.851 0.120 15 89320857 missense variant G/A snv 6.8E-04 3.4E-04 4
rs121908450
RANBP2 ; EDAR
0.851 0.160 2 108929288 missense variant C/T snv 4.0E-06 1.4E-05 4
rs138929605
POLG
0.882 0.080 15 89330106 missense variant T/A;C;G snv 3.8E-04; 2.0E-05 3
rs145843073
MIR6766 ; POLG
0.882 0.080 15 89327198 missense variant T/C snv 4.7E-04 6.3E-04 2
rs121918056
POLG
0.882 0.080 15 89330257 missense variant G/A snv 4.0E-06 7.0E-06 2
rs139590686
POLG
0.925 0.080 15 89321007 missense variant T/C;G snv 1.1E-04 2
rs780424781
RANBP2 ; EDAR
0.925 0.080 2 108929289 missense variant G/A;T snv 8.0E-06 7.0E-06 2
rs121918050
POLG
1.000 15 89321743 missense variant T/C snv 4.0E-06 7.0E-06 1