Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6666258
KCNN3
0.882 0.080 1 154841792 intron variant G/C snv 0.30 3
rs74577862
ADIPOQ
0.882 0.080 3 186843903 intron variant G/A snv 1.8E-02 3
rs7629265
SCN5A
0.882 0.080 3 38607330 intron variant C/T snv 2.3E-02 3
rs13447720
MRE11
0.925 0.040 11 94432160 intron variant T/C snv 0.17 2
rs16881446
HS3ST1
0.925 0.040 4 11406961 intron variant T/C snv 0.27 2
rs4142986
COL15A1
0.925 0.040 9 99052344 intron variant C/A;G;T snv 1.1E-04; 0.75; 4.0E-06 2
rs499952
MRE11
0.925 0.040 11 94449826 intron variant G/T snv 0.41 2
rs6918289
ADCY10P1
0.925 0.040 6 41134089 intron variant G/T snv 9.8E-02 2
rs7177922
RYR3
0.925 0.040 15 33616418 intron variant G/A snv 0.19 2
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 6
rs8042271 0.882 0.040 15 89030987 intergenic variant G/A;T snv 3
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs4552883 0.925 0.040 8 139234730 regulatory region variant G/A;C snv 2
rs67608943
PCSK9
0.851 0.080 1 55046549 stop gained C/G;T snv 1.9E-04 8
rs28362286
PCSK9
0.851 0.080 1 55063542 stop gained C/A;T snv 5.6E-04 6
rs750996166
USF1
0.925 0.040 1 161041409 stop gained G/A snv 4.0E-06 7.0E-06 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249