Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17008504 1.000 0.160 4 124718662 intergenic variant T/A snv 4.3E-02 1
rs2271100
AGA
1.000 0.160 4 177438525 intron variant T/C snv 0.19 1
rs2157257
MYH9
1.000 0.160 22 36312293 intron variant A/G snv 0.52 1
rs6056923
PAK5
1.000 0.160 20 9840271 intron variant T/C snv 0.10 1
rs114580964
PRRC2A
1.000 0.160 6 31636736 missense variant C/A;T snv 3.4E-03 1.4E-03 1
rs1364989 0.925 0.160 4 54145602 intron variant T/C snv 0.73 2
rs601162 0.925 0.160 9 29632144 upstream gene variant A/C;G;T snv 2
rs6697139 0.925 0.160 1 161690906 intergenic variant G/A;T snv 2
rs7692514 0.925 0.160 4 65276878 intergenic variant G/A;C snv 2
rs7773456 0.925 0.160 6 19823007 intron variant T/G snv 0.35 2
rs1108131
CAMK1D
0.925 0.160 10 12455748 intron variant T/C snv 0.28 2
rs958476
LOC107984410 ; BARX2
0.925 0.160 11 129451923 3 prime UTR variant T/A;G snv 2
rs7834765
LOC107986971
0.925 0.160 8 121263666 regulatory region variant G/T snv 0.32 2
rs8012283
NIN
0.925 0.160 14 50767442 intron variant A/G snv 0.23 2
rs1635564
PADI4
0.925 0.160 1 17357031 intron variant T/A;G snv 2
rs3792192
PLA2R1
0.925 0.160 2 160030364 intron variant G/A snv 0.35 2
rs11057864
SCARB1
0.925 0.160 12 124851404 intron variant C/A snv 6.5E-02 2
rs274068
SLC5A11
0.925 0.160 16 24887651 intron variant C/A snv 0.74 2
rs11893826
SLC8A1
0.925 0.160 2 40337507 intron variant G/A snv 0.27 2
rs2246614
CDHR5
0.882 0.160 11 619789 missense variant T/G snv 0.63 0.59 3
rs2295415
CREM
0.882 0.160 10 35212510 3 prime UTR variant A/G snv 0.19 3
rs4984
LOC105374794 ; ADD2
0.925 0.160 2 70673271 synonymous variant G/A snv 0.12 0.15 3
rs8091180
NFATC1
1.000 0.160 18 79404243 intron variant G/A snv 0.46 3
rs11203368
PADI4
0.925 0.200 1 17340013 intron variant C/T snv 0.57 3
rs329498
PELI1
0.882 0.200 2 64100410 synonymous variant G/A;C;T snv 8.0E-06; 0.34 3