Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6801957
SCN10A
1.000 0.080 3 38725824 intron variant T/C snv 0.67 7
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 5
rs1036207
NDFIP1
1.000 0.080 5 142119476 intron variant A/G;T snv 3
rs10411936
EPS15L1
1.000 0.080 19 16437564 intron variant A/G snv 0.63 3
rs11621145
IGHA1
1.000 0.080 14 105706543 intron variant G/A snv 0.49 3
rs11949767
MXD3
1.000 0.080 5 177313243 upstream gene variant A/C;G snv 3
rs4075958
RGS14
1.000 0.080 5 177357511 upstream gene variant G/A snv 0.21 3
rs4648356
TTC34
1.000 0.080 1 2792599 intron variant C/A snv 0.39 3
rs882300
LOC107985947
1.000 0.080 2 136218685 intergenic variant T/C;G snv 3
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
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