Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1278838206
PCDH19
0.925 0.200 X 100296654 missense variant C/T snv 1.1E-05 3
rs121918364
SRPX2
0.851 0.200 X 100662227 missense variant A/C snv 3.3E-05 2.9E-05 5
rs786201003
NALCN
0.925 0.080 13 101083752 missense variant C/T snv 3
rs5030849
PAH
0.851 0.280 12 102852875 missense variant C/A;G;T snv 2.2E-04 6
rs1177566365
RIMS2
8 103766303 missense variant G/T snv 4.0E-06 7.0E-06 1
rs187438258
MYHAS ; MYH2
17 10525806 missense variant G/A snv 8.6E-04 1.9E-04 2
rs202198533
MYH2 ; MYHAS
17 10533547 missense variant C/T snv 1.6E-04 1.0E-04 2
rs551253128
MID2 ; LOC101928335
X 107905581 missense variant A/G snv 1.3E-03 1.6E-04 1
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs886041761
KCNA2
0.925 0.200 1 110603902 missense variant C/T snv 6
rs267607048
SHOC2
0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 16
rs1301796529
LDLR ; MIR6886
19 11113444 missense variant C/G snv 4.0E-06 1
rs121434612
PAK3
1.000 0.080 X 111142119 missense variant C/T snv 2
rs121434613
PAK3
0.882 0.240 X 111194402 missense variant C/A snv 4
rs121434614
PAK3
0.925 0.200 X 111196570 missense variant G/C snv 3
rs1445362103
ARHGEF7
1.000 0.040 13 111244248 missense variant T/C snv 1.2E-05 7.0E-06 2
rs863225264
MTOR
0.827 0.240 1 11130747 missense variant C/T snv 6
rs150263896
ZBTB20
3 114339010 missense variant C/T snv 1.1E-05 7.0E-06 1
rs879255635
ZBTB20
3 114339384 missense variant G/A snv 1
rs1335072648
RAD21
1.000 0.200 8 116854423 missense variant C/T snv 4.0E-06 2
rs4846049
C1orf167 ; MTHFR
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 10
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614