Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1127379
SFRP1
0.882 0.120 8 41263761 3 prime UTR variant T/C snv 0.48 3
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11409738
DYNC1I1
1.000 0.040 7 96090522 intron variant A/-;AA;AAA;AAAA delins 1
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1149620
TSKU
1.000 0.040 11 76795528 intron variant T/A snv 0.50 1
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11564299 0.925 0.040 18 28180064 upstream gene variant A/G snv 0.17 2
rs115740542
H2AC6 ; H2BC4
0.925 0.040 6 26123274 intron variant T/C snv 3.6E-02 2
rs116855380 1.000 0.040 20 47491550 downstream gene variant A/G snv 2.8E-02 1
rs11688000
TACR1
1.000 0.040 2 75066030 intron variant A/G snv 0.34 1
rs11718863
COL6A4P1
0.882 0.080 3 15175196 non coding transcript exon variant A/G;T snv 0.21 3
rs11807350
ADAMTS4
1.000 0.040 1 161191145 missense variant C/T snv 3.1E-04 4.7E-04 1
rs11842874
MCF2L
1.000 0.040 13 113040195 intron variant A/G snv 0.12 1
rs1194611372
S100A11
0.763 0.320 1 152032679 missense variant A/C snv 9
rs11965969
NT5DC1 ; COL10A1
1.000 0.040 6 116131040 intron variant T/G snv 0.50 1
rs12102171
SMAD3
1.000 0.040 15 67132695 intron variant C/T snv 0.22 1
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 8
rs12154055 1.000 0.040 6 44481960 intergenic variant G/A snv 0.27 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913474
FGFR2
0.790 0.200 10 121515260 missense variant A/G snv 9
rs121918505
FGFR2
0.851 0.080 10 121520119 missense variant A/G snv 5
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1254566330
MOK
0.925 0.120 14 102250845 stop gained C/T snv 7.0E-06 2