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: rs10738760
rs10738760 		7 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 0.010 1.000 1 2019 2019
dbSNP: rs115523882
rs115523882 		1 1.000 0.160 3 168158417 intergenic variant A/G snv 9.5E-03 0.700 1.000 1 2019 2019
dbSNP: rs5498
rs5498
ICAM1 ; ICAM4
99 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.010 1.000 1 2008 2008
dbSNP: rs74161190
rs74161190 		1 1.000 0.160 10 130737530 intergenic variant A/G snv 1.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs74705672
rs74705672
OC90
1 1.000 0.160 8 132042380 intron variant A/T snv 4.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs201584991
rs201584991
ZNF572
1 1.000 0.160 8 124979483 downstream gene variant ATT/- delins 2.6E-04 0.700 1.000 1 2019 2019
dbSNP: rs78340493
rs78340493 		1 1.000 0.160 4 43636179 intergenic variant C/A snv 5.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs78464534
rs78464534
DPP10
1 1.000 0.160 2 115234275 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs1617640
rs1617640
EPO
15 0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs1902491
rs1902491 		2 0.925 0.240 4 155134181 intergenic variant C/A;T snv 0.010 1.000 1 2018 2018
dbSNP: rs1414474
rs1414474
C1orf94
1 1.000 0.160 1 34197810 missense variant C/G snv 0.20 0.20 0.700 1.000 1 2019 2019
dbSNP: rs1801282
rs1801282
PPARG
131 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2013 2013
dbSNP: rs1805192
rs1805192
PPARG
121 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2013 2013
dbSNP: rs2910164
rs2910164
MIR146A ; MIR3142HG
193 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 0.010 1.000 1 2016 2016
dbSNP: rs11201335
rs11201335 		1 1.000 0.160 10 85018443 intergenic variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
226 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2003 2003
dbSNP: rs1800471
rs1800471
TGFB1
48 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 0.010 1.000 1 2002 2002
dbSNP: rs2064196
rs2064196 		1 1.000 0.160 6 144266047 intergenic variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1000708
rs1000708
SLC16A7
1 1.000 0.160 12 59689707 intron variant C/T snv 0.58 0.700 1.000 1 2019 2019
dbSNP: rs11488711
rs11488711
LINC02815 ; LINC02814
1 1.000 0.160 1 229105486 intron variant C/T snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs138683663
rs138683663 		1 1.000 0.160 18 59195550 intergenic variant C/T snv 4.2E-03 0.700 1.000 1 2019 2019
dbSNP: rs184340784
rs184340784 		2 0.925 0.160 1 4529823 intergenic variant C/T snv 6.1E-04 0.700 1.000 1 2019 2019
dbSNP: rs4865047
rs4865047
CEP135
2 0.925 0.240 4 55955640 intron variant C/T snv 0.12 0.010 1.000 1 2018 2018
dbSNP: rs61811867
rs61811867
KCNN3
1 1.000 0.160 1 154802768 intron variant C/T snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs114921230
rs114921230
STUM
1 1.000 0.160 1 226595161 intron variant G/A snv 3.6E-02 0.700 1.000 1 2019 2019