Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs2074192
ACE2
0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs2106809
ACE2
0.827 0.120 X 15599938 intron variant A/G snv 0.19 8
rs1436109
NCAM1
1.000 0.080 11 113120896 intron variant G/T snv 8.5E-02 3
rs4966014
IGF1R
0.882 0.200 15 98704789 intron variant C/G;T snv 3
rs17132261
TMEM232
1.000 0.080 5 110672513 intron variant C/T snv 4.8E-02 2
rs2292462
NMB
1.000 0.080 15 84657523 intron variant G/C;T snv 2
rs10500279
RYR1
1.000 0.080 19 38544428 intron variant G/C snv 5.6E-02 1
rs1957757
HIF1A-AS3 ; HIF1A
1.000 0.080 14 61730230 intron variant T/C snv 0.74 1
rs1974201
ENPP1
1.000 0.080 6 131889981 intron variant G/A;C;T snv 1
rs2071090
RYR1
1.000 0.080 19 38524814 intron variant T/C snv 0.15 1
rs2960321
RYR1
1.000 0.080 19 38557523 intron variant C/A snv 0.18 1
rs4129218
LOC100507065
1.000 0.080 12 65564881 intron variant G/A snv 0.70 1
rs75404003
TNFRSF11A
1.000 0.080 18 62361277 intron variant C/- delins 1
rs756529
KCNB1 ; LOC105372649
1.000 0.080 20 49394471 intron variant G/A snv 0.44 1
rs9402349
ENPP1
1.000 0.080 6 131863968 intron variant A/C snv 9.8E-02 1
rs9594782
TNFSF11
1.000 0.080 13 42577050 intron variant T/C snv 4.0E-02 1
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs397516005
MYBPC3
0.827 0.120 11 47333566 stop gained G/A snv 8.4E-06 2.8E-05 5
rs387907267
MYBPC3
0.851 0.120 11 47335120 stop gained G/A snv 1.2E-05 2.8E-05 4
rs397516037
MYBPC3
0.851 0.120 11 47332189 stop gained G/A snv 8.0E-06 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134