Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9990514 1.000 0.040 4 187920994 intergenic variant T/C snv 0.21 2
rs996414 1.000 0.040 9 26580069 intergenic variant G/A snv 0.76 1
rs9944155
SERPINA1
1.000 0.040 14 94377162 3 prime UTR variant C/T snv 4.3E-03 1
rs9928486
PRKCB
1.000 0.040 16 24076855 intron variant T/C snv 1.4E-02 2
rs9898686 1.000 0.040 17 71077051 intergenic variant C/T snv 0.31 1
rs9859058
LINC00886
1.000 0.040 3 156795028 intron variant C/A snv 0.39 2
rs9847124 0.925 0.120 3 152872973 intergenic variant T/G snv 0.14 2
rs979453
CCDC69 ; GM2A ; LOC105378230
1.000 0.040 5 151215512 intron variant A/G snv 0.44 1
rs9788721
HYKK
1.000 0.040 15 78510527 intron variant C/T snv 0.65 6
rs975278
SERPINE2
0.925 0.040 2 223982990 intron variant T/A;C snv 2
rs9686327 1.000 0.040 5 15018428 intergenic variant G/A;T snv 1
rs965604
IREB2
1.000 0.040 15 78496881 intron variant G/A snv 0.50 4
rs9617650
MICAL3
1.000 0.040 22 18006117 non coding transcript exon variant G/C snv 0.19 1
rs9599114
PCDH9
1.000 0.040 13 66412999 intron variant T/C snv 0.34 1
rs9590614
VWA8
1.000 0.040 13 41601452 intron variant G/C snv 0.31 1
rs9554314
FLT1
0.851 0.080 13 28301652 3 prime UTR variant A/C snv 4
rs955277 1.000 0.040 2 9150228 downstream gene variant C/A;T snv 1
rs9534578
LOC105370195
0.925 0.080 13 47269242 intergenic variant C/A snv 0.11 2
rs9525927 0.925 0.160 13 44268367 regulatory region variant G/A snv 0.80 2
rs951266
CHRNA5
0.882 0.080 15 78586199 intron variant G/A snv 0.26 6
rs950063 1.000 0.040 4 125510764 downstream gene variant C/T snv 0.71 1
rs9486594
PDSS2
1.000 0.040 6 107351323 intron variant T/A;C snv 1
rs9435731
MFAP2
1.000 0.040 1 16979534 intron variant C/A snv 0.40 1
rs943306
ASTN2
1.000 0.040 9 116862396 intron variant C/T snv 0.48 1
rs9403391 1.000 0.040 6 142493854 intergenic variant C/T snv 4.6E-02 1