Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10500264 1.000 0.080 19 33259408 intergenic variant G/A snv 0.14 2
rs11609
IQGAP1
1.000 0.080 15 90500533 3 prime UTR variant C/G snv 0.42 2
rs12115114 1.000 0.080 8 63477322 non coding transcript exon variant A/G;T snv 2
rs12487066
LOC105374027
1.000 0.080 3 106193283 intron variant T/C snv 0.28 2
rs12988804
LRP2
1.000 0.080 2 169261301 intron variant C/T snv 0.24 2
rs1398607 1.000 0.080 3 102036894 TF binding site variant C/A;T snv 2
rs148038936
ITGB2 ; LOC107987303
1.000 0.080 21 44910354 missense variant G/A;C snv 2.4E-05; 1.6E-04 2
rs1517440
LOC105373895
1.000 0.080 2 220589153 intron variant T/C;G snv 2
rs17066096 1.000 0.080 6 137131771 intergenic variant A/G snv 0.20 2
rs17519972
GLMN ; RPAP2
1.000 0.080 1 92362948 intron variant A/C snv 0.15 2
rs17758761
ANKFN1
1.000 0.080 17 55977164 intron variant A/C snv 4.1E-02 2
rs1801406
BRCA2
1.000 0.080 13 32337751 missense variant A/C;G snv 0.29 2
rs184607650
EIF2B4
1.000 0.080 2 27367140 missense variant G/C snv 5.1E-04 4.7E-04 2
rs1920296
IQCB1
1.000 0.080 3 121824730 intron variant A/C;G snv 2
rs2037815
CASP8
0.925 0.080 2 201236992 intron variant G/A snv 0.55 2
rs210131
GGNBP1
1.000 0.080 6 33567689 intron variant T/C snv 0.95 2
rs2236262
ZFP36L1
1.000 0.080 14 68794755 intron variant A/G snv 0.45 2
rs2371108
EOMES
1.000 0.080 3 27715527 downstream gene variant G/T snv 0.42 2
rs2412973
HORMAD2
1.000 0.080 22 30133642 intron variant C/A snv 0.54 2
rs2688608 1.000 0.080 10 73898591 regulatory region variant G/T snv 0.44 2
rs290986
SYK
1.000 0.080 9 90801254 upstream gene variant A/G snv 0.18 2
rs305217
PKN2
1.000 0.080 1 88754789 intron variant G/A snv 8.6E-02 2
rs307896
SAE1
1.000 0.080 19 47158236 intron variant G/A;C snv 2
rs3130000
DHX16
1.000 0.080 6 30660305 non coding transcript exon variant A/G;T snv 2
rs338610
LINC01967
1.000 0.080 3 28039951 intron variant A/G snv 0.73 2