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: rs128738
rs128738
P4HA2
2 0.925 0.160 5 132205182 intron variant G/T snv 0.18 0.700 1.000 1 2017 2017
dbSNP: rs4252134
rs4252134
PLG
2 0.925 0.160 6 160732495 intron variant T/C snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs477515
rs477515
HLA-DRB1
10 0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 0.700 1.000 1 2015 2015
dbSNP: rs6679677
rs6679677
PHTF1
26 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs9268905
rs9268905
HLA-DRB9
2 0.925 0.280 6 32464300 intron variant G/C snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs9275592
rs9275592 		2 0.925 0.200 6 32712843 regulatory region variant G/T snv 9.1E-02 0.700 1.000 1 2017 2017