Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 13
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 10
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 8
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 8
rs247616 1.000 0.040 16 56955678 intergenic variant C/T snv 0.29 8
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 8
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 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
rs2000999
HPR ; TXNL4B
1.000 0.080 16 72074194 intron variant G/A snv 0.16 7
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 6
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 6
rs12042319
DOCK7
1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36 6