Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12695895
AGTR1
0.925 0.040 3 148725481 intron variant C/T snv 0.31 3
rs764522
TGFBR2 ; LOC105377015
0.882 0.080 3 30605058 upstream gene variant G/A;C snv 3
rs1036095
TGFBR2
1.000 0.040 3 30620836 intron variant C/G snv 0.72 1
rs767169659
MYLK
1.000 0.040 3 123733800 missense variant G/A snv 1.2E-05 1
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs121917864
TLR2
0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 12
rs3877899
CCDC152 ; SELENOP
0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20 7
rs7579
CCDC152 ; SELENOP
0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26 6
rs326118
MTRR ; FASTKD3
0.925 0.080 5 7868430 intron variant T/G snv 0.21 2
rs2652106
VCAN
1.000 0.040 5 83498217 intron variant G/T snv 0.39 1
rs12191786
CASC15
0.851 0.120 6 22004398 intron variant C/A;T snv 4
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs1419338705
ELN
1.000 0.040 7 74048163 missense variant C/T snv 7.0E-06 1
rs782591769
ELN
1.000 0.040 7 74045237 missense variant G/C snv 8.0E-06 1
rs3019885
SLC30A8
0.925 0.120 8 117013406 intron variant T/A;G snv 2
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
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs7025486
DAB2IP
0.851 0.040 9 121660124 intron variant G/A snv 0.28 4
rs7866503
CDKN2B-AS1
0.882 0.080 9 22091925 intron variant G/T snv 0.50 3
rs10758278
PHF24
1.000 0.040 9 34825306 intron variant G/A snv 0.53 1
rs10985349
DAB2IP
1.000 0.040 9 121662964 intron variant C/T snv 0.17 1