Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs1761667
CD36
0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs1466535
LRP1
0.790 0.160 12 57140687 intron variant G/A;C snv 9
rs2074192
ACE2
0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs16933090
SOX6
0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7
rs2026458
PHACTR1
0.882 0.080 6 12825642 intron variant C/T snv 0.34 6
rs702553
PDE4D
0.882 0.160 5 60440946 intron variant A/T snv 0.37 6
rs7439293
PALLD
0.807 0.080 4 168756335 non coding transcript exon variant G/A snv 0.44 6
rs9632884
CDKN2B-AS1
0.851 0.160 9 22072302 intron variant G/A;C snv 6
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
rs17477177 1.000 0.080 7 106771412 upstream gene variant T/C snv 0.17 4
rs877087
RYR3
0.882 0.080 15 33582074 intron variant T/C;G snv 4
rs879922
ACE2
0.882 0.160 X 15572684 intron variant C/G snv 4
rs12998782
MARCO
0.882 0.160 2 118967804 intron variant C/T snv 0.19 3
rs28357094
SPP1
0.882 0.160 4 87975645 non coding transcript exon variant T/G snv 0.17 3
rs74577862
ADIPOQ
0.882 0.080 3 186843903 intron variant G/A snv 1.8E-02 3