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: rs10007052
rs10007052
RNF150
1 1.000 0.040 4 141084419 intron variant C/A snv 0.31 0.710 1.000 2 2012 2015
dbSNP: rs16865421
rs16865421
SERPINE2
1 1.000 0.040 2 223993376 intron variant A/G snv 0.10 0.020 1.000 2 2009 2019
dbSNP: rs2806356
rs2806356
ARMC2
1 1.000 0.040 6 108945052 intron variant T/C;G snv 0.700 1.000 2 2017 2019
dbSNP: rs3024791
rs3024791
SFTPB
1 1.000 0.040 2 85668581 intron variant C/T snv 0.17 0.020 0.500 2 2008 2011
dbSNP: rs584367
rs584367
PLA2G2D
1 1.000 0.040 1 20115561 missense variant T/C snv 0.66 0.70 0.020 1.000 2 2005 2009
dbSNP: rs647097
rs647097
MTCL1
1 1.000 0.040 18 8808466 intron variant T/C snv 0.31 0.700 1.000 2 2017 2019
dbSNP: rs6957
rs6957
TGFB1 ; CCDC97
1 1.000 0.040 19 41324701 3 prime UTR variant T/C snv 0.21 0.020 1.000 2 2012 2017
dbSNP: rs9296092
rs9296092 		1 1.000 0.040 6 33510719 intergenic variant A/G snv 0.55 0.810 1.000 2 2011 2017
dbSNP: rs10013495
rs10013495 		1 1.000 0.040 4 144584486 intron variant C/T snv 0.23 0.010 1.000 1 2013 2013
dbSNP: rs1002149
rs1002149
GSR ; UBXN8
1 1.000 0.040 8 30728221 upstream gene variant G/T snv 0.20 0.010 1.000 1 2019 2019
dbSNP: rs10037493
rs10037493
HTR4 ; LOC107986462
1 1.000 0.040 5 148475407 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10056066
rs10056066
SGCD
1 1.000 0.040 5 156434616 intron variant G/A snv 2.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs10076733
rs10076733
IRF1-AS1 ; LINC02863
1 1.000 0.040 5 132425039 intron variant G/T snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs10114763
rs10114763
GLIS3
1 1.000 0.040 9 4143749 intron variant A/T snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs10152300
rs10152300
ADAMTSL3
1 1.000 0.040 15 83724155 intron variant G/A snv 0.84 0.700 1.000 1 2019 2019
dbSNP: rs10279301
rs10279301
LINC01006
1 1.000 0.040 7 156468621 intron variant C/T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs1038376
rs1038376
CYP2B6
1 1.000 0.040 19 41018104 3 prime UTR variant A/T snv 0.31 0.010 1.000 1 2019 2019
dbSNP: rs10491678
rs10491678 		1 1.000 0.040 9 29568688 intergenic variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs1051052
rs1051052
SERPINA1
1 1.000 0.040 14 94377595 3 prime UTR variant A/G snv 0.47 0.010 1.000 1 2018 2018
dbSNP: rs10519225
rs10519225
FGF7 ; FAM227B
1 1.000 0.040 15 49428581 intron variant G/A snv 0.28 0.010 1.000 1 2012 2012
dbSNP: rs1059823
rs1059823
SLC11A1
1 1.000 0.040 2 218395121 3 prime UTR variant A/G snv 0.52 0.010 1.000 1 2008 2008
dbSNP: rs10760580
rs10760580 		1 1.000 0.040 9 98899368 TF binding site variant G/A snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs1080879
rs1080879 		1 1.000 0.040 5 15054693 intergenic variant T/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs10873142
rs10873142
HIF1A ; HIF1A-AS3
1 1.000 0.040 14 61736744 intron variant C/T snv 0.67 0.010 1.000 1 2018 2018
dbSNP: rs10890311
rs10890311
RNF220
1 1.000 0.040 1 44602096 intron variant C/T snv 0.22 0.700 1.000 1 2019 2019