Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174567
FADS1 ; FADS2
1.000 0.080 11 61825533 intron variant A/G;T snv 4
rs174580
FADS2
1.000 0.080 11 61839170 intron variant A/C;G snv 4
rs174581
FADS2
0.925 0.160 11 61839211 intron variant G/A;C snv 4
rs174592
FADS2
1.000 0.080 11 61851136 intron variant A/G snv 0.44 4
rs2279463
SLC22A2
1.000 0.080 6 160247357 intron variant A/G;T snv 4
rs2467853
SPATA5L1
1.000 0.080 15 45406595 intron variant T/A;G snv 4
rs2928148
INO80
15 41109352 intron variant G/A snv 0.44 4
rs347685
TFDP2
1.000 0.080 3 142088295 intron variant C/A snv 0.74 4
rs4730751
CAV1
0.882 0.120 7 116540796 intron variant C/A snv 0.22 4
rs4744712
PIP5K1B
1.000 0.080 9 68819791 intron variant A/C;T snv 4
rs491567
WDR72
1.000 0.080 15 53654396 intron variant A/C snv 0.34 4
rs6431731
LINC01804
1.000 0.080 2 15722878 intron variant C/T snv 0.97 4
rs9319428
FLT1
0.925 0.080 13 28399484 intron variant G/A snv 0.30 4
rs1077989
GPHN ; TMEM229B
1.000 0.080 14 67509105 intron variant A/C snv 0.39 3
rs12124078
DNAJC16
1 15543404 intron variant A/G snv 0.32 3
rs174562
FADS2 ; FADS1
1.000 0.080 11 61817672 intron variant A/G snv 0.28 3
rs174578
FADS2
1.000 0.080 11 61838027 intron variant T/A snv 0.38 3
rs6066043
SLC13A3
1.000 0.080 20 46659814 intron variant G/A;T snv 3
rs7252778
SLC7A9
1.000 0.080 19 32869463 intron variant C/A;T snv 3
rs7943728
MYRF ; TMEM258
1.000 0.080 11 61779596 intron variant G/A snv 0.12 0.11 3
rs99780
FADS1 ; FADS2
1.000 0.080 11 61829161 intron variant C/T snv 0.38 3
rs1020120
LOC102724036
1.000 0.080 9 84611173 intron variant C/T snv 0.60 2
rs11011653
PLXDC2
1.000 0.080 10 19875064 intron variant A/G;T snv 2
rs11078903
CDK12
17 39475671 intron variant G/A;C;T snv 2
rs112201728
SLC22A1
1.000 0.080 6 160130454 intron variant C/A;T snv 2