Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7114303
SBF2
1.000 0.040 11 10074140 intron variant G/C snv 0.28 1
rs12150284
GAS7
1.000 0.040 17 10127773 intron variant C/A;G;T snv 3
rs9913911
GAS7
0.925 0.040 17 10127866 intron variant A/G snv 0.32 4
rs11656696
GAS7
0.882 0.040 17 10130362 intron variant C/A snv 0.36 5
rs869833
TMEM182
1.000 0.040 2 102766672 intron variant T/C snv 0.49 1
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs3753841
COL11A1
0.827 0.080 1 102914362 missense variant G/A snv 0.61 0.49 7
rs2437812
LOC105376196
1.000 0.040 9 104930920 upstream gene variant A/C;T snv 1
rs2472496
LOC105376196
1.000 0.040 9 104933072 upstream gene variant G/A snv 0.61 2
rs2472493
LOC105376196
0.851 0.040 9 104933567 downstream gene variant G/A snv 0.61 5
rs284489
ZFPM2
0.882 0.080 8 104945792 intron variant A/G snv 0.45 3
rs2022945 1.000 0.040 8 107238911 intergenic variant A/G snv 0.87 2
rs10505100
ANGPT1
1.000 0.040 8 107266388 intron variant C/A snv 0.13 1
rs1438561194
WDR36
1.000 0.040 5 111092304 missense variant G/A snv 4.0E-06 7.0E-06 1
rs10038177
WDR36
0.925 0.040 5 111100751 intron variant C/T snv 0.53 0.54 3
rs35703638
WDR36
1.000 0.040 5 111106140 missense variant G/A snv 8.3E-03 4.1E-03 1
rs13178997
WDR36
0.925 0.040 5 111108550 intron variant G/A;T snv 2
rs116529882
WDR36
0.925 0.040 5 111110280 missense variant G/A snv 7.5E-04 8.9E-04 2
rs34595252
WDR36
0.925 0.040 5 111119021 missense variant A/G snv 4.3E-03 4.5E-03 2
rs197388
INKA2 ; DDX20 ; LOC101928718
0.925 0.040 1 111754860 non coding transcript exon variant A/T snv 0.27 2
rs12699251
THSD7A
1.000 0.040 7 11639486 intron variant A/G snv 0.33 1
rs10281637 1.000 0.040 7 116511284 downstream gene variant T/C snv 0.28 2
rs2024211 1.000 0.040 7 116512971 downstream gene variant A/C snv 0.27 1
rs12377632
TLR4
0.827 0.120 9 117710452 intron variant T/A;C snv 5
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14