Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11864909
PDILT
0.851 0.160 16 20389517 intron variant C/T snv 0.23 7
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 7
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 7
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs3834458
FADS1 ; FADS2
0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs452204
IL1RN
0.807 0.200 2 113131484 intron variant G/A snv 0.45 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 7
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 7
rs1171616
SLC16A9
0.882 0.200 10 59708831 intron variant G/T snv 0.79 6
rs4976646
RGS14
0.851 0.200 5 177361569 intron variant T/C snv 0.41 6
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs10951982
RAC1
0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs17319721
SHROOM3
0.925 0.080 4 76447694 intron variant G/A snv 0.34 5
rs174528
TMEM258 ; MYRF
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 5
rs2823139 1.000 0.080 21 15204463 intron variant G/A snv 0.34 5
rs28456
FADS1 ; FADS2
0.925 0.120 11 61822009 intron variant A/C;G snv 5
rs3812036
SLC34A1
0.925 0.120 5 177386403 intron variant C/T snv 0.23 0.20 5
rs4148155
ABCG2
0.882 0.200 4 88133515 intron variant A/G snv 8.7E-02 5
rs626277
DACH1
1.000 0.080 13 71773564 intron variant A/C snv 0.51 5
rs6420094
SLC34A1
1.000 0.080 5 177390635 intron variant A/G snv 0.29 5
rs7394579
FADS2 ; FADS1
1.000 0.080 11 61813978 intron variant A/G snv 0.22 5
rs7805747
PRKAG2
1.000 0.080 7 151710715 intron variant G/A snv 0.26 5
rs8096658
NFATC1 ; LOC107985163
0.925 0.120 18 79396537 intron variant C/G snv 0.39 5