Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112329286
SYNE2
1.000 0.080 14 63773159 intron variant -/ATTT delins 0.24 4
rs59834205
SLC2A9
0.882 0.200 4 9959396 intron variant -/GA delins 1.1E-04 3
rs35473591
FADS2 ; FADS1
1.000 0.080 11 61818856 intron variant -/T delins 0.28 2
rs16347
IL1A
0.925 0.080 2 112774138 3 prime UTR variant -/TGAA delins 0.70 2
rs5792235
FADS2 ; FADS1
1.000 0.080 11 61828851 intron variant A/- delins 0.30 2
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs626277
DACH1
1.000 0.080 13 71773564 intron variant A/C snv 0.51 5
rs491567
WDR72
1.000 0.080 15 53654396 intron variant A/C snv 0.34 4
rs75444904
HPR ; TXNL4B
0.851 0.160 16 72061751 intron variant A/C snv 2.4E-02 4
rs1077989
GPHN ; TMEM229B
1.000 0.080 14 67509105 intron variant A/C snv 0.39 3
rs1933182 1.000 0.080 1 109457216 intergenic variant A/C snv 0.63 3
rs2490391
SDCCAG8
1.000 0.080 1 243306367 3 prime UTR variant A/C snv 0.50 2
rs730947 0.925 0.080 2 218838575 upstream gene variant A/C snv 1.0E-01 2
rs117329947
LOC105369957 ; C12orf75
1.000 0.080 12 105391125 intron variant A/C snv 2.2E-02 1
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs28456
FADS1 ; FADS2
0.925 0.120 11 61822009 intron variant A/C;G snv 5
rs174580
FADS2
1.000 0.080 11 61839170 intron variant A/C;G snv 4
rs12137135 0.925 0.080 1 22348728 intergenic variant A/C;G snv 2
rs145640112
KLKB1
0.925 0.080 4 186250267 missense variant A/C;G snv 1.8E-04; 4.0E-06 2
rs1989248 1.000 0.080 7 148443990 upstream gene variant A/C;G snv 1
rs174557
FADS2 ; FADS1
1.000 0.080 11 61813896 intron variant A/C;G;T snv 2
rs4744712
PIP5K1B
1.000 0.080 9 68819791 intron variant A/C;T snv 4
rs594442 1.000 0.080 6 93138166 intergenic variant A/C;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614