Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 7
rs8756
HMGA2
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 7
rs17265513
ZHX3
0.925 0.160 20 41203988 missense variant T/C snv 0.14 0.14 6
rs12889267
ARHGEF40
14 21074607 missense variant A/G snv 0.16 0.13 4
rs2955083
EEFSEC
1.000 0.040 3 128242335 intron variant T/A snv 0.89 4
rs3749237
IP6K1
3 49732599 intron variant G/A snv 0.26 4
rs17287293
LOC105369698
1.000 0.080 12 24617944 intergenic variant A/G snv 0.12 4
rs365990
MYH6
1.000 0.080 14 23392602 missense variant A/G snv 0.34 0.45 4
rs7612445 1.000 0.080 3 179455191 upstream gene variant G/T snv 0.24 3
rs4608502
COL4A3 ; MFF-DT
2 227269439 intron variant T/A;C snv 3
rs452036
MYH6
14 23396676 intron variant G/A;C snv 0.33 3
rs12501032
PPARGC1A
0.925 0.120 4 23949395 regulatory region variant C/G snv 0.20 3
rs174536
TMEM258 ; MYRF
11 61784455 non coding transcript exon variant A/C snv 0.29 3
rs3791979
TNS1
1.000 0.040 2 217802649 3 prime UTR variant T/A;C;G snv 3
rs57942103
ZFPM2
1.000 0.040 8 105501233 intron variant A/C snv 0.25 3
rs1158317 1.000 0.040 6 120626545 intron variant C/T snv 0.58 2
rs12173787 1.000 0.040 6 33767694 downstream gene variant G/C snv 0.51 2
rs56233017 8 143907320 regulatory region variant G/A snv 2.7E-02 2
rs7143026 1.000 0.040 14 65784238 intergenic variant A/G snv 0.38 2
rs7449334
ADGRV1
1.000 0.040 5 91046595 intron variant G/A;C snv 0.76 2
rs12721051
APOC1
19 44918903 3 prime UTR variant C/G snv 0.14 0.15 2