Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11413744 1.000 0.080 4 147474132 intergenic variant -/T delins 0.15 1
rs4897549 1.000 0.080 6 131898350 upstream gene variant C/T snv 0.30 1
rs113309773
CFDP1
1.000 0.080 16 75398788 intron variant -/A;C ins 0.51 1
rs4675095
IRS1
1.000 0.080 2 226787251 intron variant A/T snv 5.3E-02 1
rs2876300
PHACTR1
1.000 0.080 6 12893871 intron variant A/C;G snv 1
rs367650109
PTGS2
1.000 0.080 1 186675959 missense variant A/G snv 4.0E-06 2.1E-05 1
rs200495339
SMARCA4
1.000 0.080 19 11078623 intron variant G/- delins 0.12 1
rs259140
STEAP2-AS1
1.000 0.080 7 89995033 intron variant T/G snv 0.79 1
rs4779614
TMCO5B
1.000 0.080 15 33247916 upstream gene variant T/C snv 0.72 1
rs7265169
TRIB3
1.000 0.080 20 384103 intron variant C/A;T snv 1
rs757818668
PTX3 ; VEPH1
0.925 0.120 3 157442729 missense variant G/A snv 1.2E-05 2
rs74577862
ADIPOQ
0.882 0.080 3 186843903 intron variant G/A snv 1.8E-02 3
rs650439
KL
1.000 0.080 13 33061802 intron variant T/A snv 0.82 0.81 3
rs12998782
MARCO
0.882 0.160 2 118967804 intron variant C/T snv 0.19 3
rs771479424
PCSK9
0.882 0.120 1 55052764 stop gained A/G;T snv 1.2E-05 3
rs28357094
SPP1
0.882 0.160 4 87975645 non coding transcript exon variant T/G snv 0.17 3
rs17477177 1.000 0.080 7 106771412 upstream gene variant T/C snv 0.17 4
rs879922
ACE2
0.882 0.160 X 15572684 intron variant C/G snv 4
rs877087
RYR3
0.882 0.080 15 33582074 intron variant T/C;G snv 4
rs17128183 0.882 0.120 14 55112795 intergenic variant A/G snv 0.57 5
rs2274273
DLGAP5
0.882 0.120 14 55147918 downstream gene variant G/A snv 0.40 5
rs774439908
MIR6886 ; LDLR
0.827 0.160 19 11113348 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 5
rs371237692
REN
0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05 5
rs9632884
CDKN2B-AS1
0.851 0.160 9 22072302 intron variant G/A;C snv 6
rs7439293
PALLD
0.807 0.080 4 168756335 non coding transcript exon variant G/A snv 0.44 6