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
rs35473591
FADS2 ; FADS1
1.000 0.080 11 61818856 intron variant -/T delins 0.28 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
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
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
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
rs730882222
SLC13A5
0.925 0.040 17 6707026 splice donor variant A/C snv 3
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
rs775077692
CETP
16 56963027 missense variant A/C;G snv 4.0E-06; 4.0E-06 1
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs174557
FADS2 ; FADS1
1.000 0.080 11 61813896 intron variant A/C;G;T snv 2
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4744712
PIP5K1B
1.000 0.080 9 68819791 intron variant A/C;T snv 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24