Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894833
RPL36A-HNRNPH2 ; GLA
0.776 0.280 X 101403984 missense variant C/G snv 1.2E-04 1.9E-05 11
rs1064794243
SCN4A
0.851 0.200 17 63941169 missense variant A/T snv 5
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs11549029
PROSER3 ; HSPB6
19 35756950 missense variant G/A snv 8.9E-04 1.3E-03 1
rs11568023
AGT
1 230712433 intron variant G/A;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909298
SGCD
0.925 0.040 5 156595000 missense variant T/G snv 2.0E-04 1.3E-04 4
rs121918460
PTPN11
0.708 0.400 12 112450364 missense variant T/A;G snv 4.0E-06 27
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs137854602
SCN5A
0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 5
rs137854607
SCN5A
0.882 0.120 3 38554309 missense variant C/G;T snv 5
rs139794067
MYL3
0.925 0.080 3 46860813 missense variant G/A;C;T snv 7.2E-05; 1.7E-04 3
rs148398509
HCN4
0.882 0.160 15 73323445 missense variant G/C snv 7.8E-03 7.2E-03 5
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1904694
PRKG1
10 51145734 intron variant A/G snv 0.45 1
rs199472968
KCNH2
0.925 0.120 7 150951484 missense variant C/T snv 3
rs216311
VWF
0.882 0.040 12 6019277 missense variant T/A;C snv 4.0E-06; 0.69 7
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs28935490
RPL36A-HNRNPH2 ; GLA
1.000 0.160 X 101398432 missense variant C/A;T snv 3.0E-03; 5.4E-06 3
rs2968857
KCNH2
1.000 0.080 7 150965242 intron variant C/T snv 0.70 2
rs3211892
CD36
1.000 0.080 7 80661053 intron variant A/G snv 0.97 0.92 2