Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 38
rs121918460
PTPN11
0.708 0.400 12 112450364 missense variant T/A;G snv 4.0E-06 27
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 11
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 10
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 4
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 4
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs137854607
SCN5A
0.882 0.120 3 38554309 missense variant C/G;T snv 3
rs59270054
LMNA
0.925 0.120 1 156115162 missense variant G/A;C snv 2
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 2
rs139794067
MYL3
0.925 0.080 3 46860813 missense variant G/A;C;T snv 7.2E-05; 1.7E-04 2
rs72546668
SSUH2 ; CAV3
0.807 0.200 3 8745644 missense variant C/A;T snv 4.0E-06; 2.6E-03 2
rs216311
VWF
0.882 0.040 12 6019277 missense variant T/A;C snv 4.0E-06; 0.69 2
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 1
rs3853601
DDX39B ; ATP6V1G2-DDX39B
1.000 0.080 6 31531826 intron variant C/G snv 0.13 1
rs199472968
KCNH2
0.925 0.120 7 150951484 missense variant C/T snv 1
rs137854602
SCN5A
0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 1