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: rs775066324
rs775066324
TIMP2
7 0.790 0.080 17 78855710 missense variant G/A;C snv 4.0E-06; 4.0E-06 0.010 < 0.001 1 2014 2014
dbSNP: rs779162432
rs779162432
PPIG
7 0.790 0.080 2 169637315 missense variant A/G snv 4.1E-06 0.010 < 0.001 1 2014 2014
dbSNP: rs7922612
rs7922612
PLCE1
14 0.752 0.080 10 94051682 intron variant C/T snv 0.39 0.010 < 0.001 1 2014 2014
dbSNP: rs909629195
rs909629195
LASP1 ; MIR6779
7 0.790 0.080 17 38914448 missense variant C/T snv 0.010 1.000 1 2016 2016
dbSNP: rs915889
rs915889
CCKAR
1 1.000 0.080 4 26484572 intron variant G/A snv 0.15 0.010 1.000 1 2013 2013
dbSNP: rs951540403
rs951540403
PLCE1
7 0.790 0.080 10 94132433 missense variant G/C snv 0.010 < 0.001 1 2014 2014