Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs28936676
rs28936676
PPOX
2 0.925 0.160 1 161170467 stop lost A/C snv 0.700 0
dbSNP: rs28936677
rs28936677
PPOX
1 1.000 0.160 1 161166882 missense variant T/C snv 2.4E-05 4.9E-05 0.700 0
dbSNP: rs121918324
rs121918324
PPOX
3 0.925 0.160 1 161167187 missense variant C/T snv 0.010 1.000 1 2000 2000
dbSNP: rs767419411
rs767419411
PPOX
3 0.882 0.200 1 161168069 missense variant G/A;C snv 1.2E-05; 8.0E-06 0.010 1.000 1 2000 2000