Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs10965780 1.000 0.040 9 23341717 intron variant C/G;T snv 3
rs12963463
TCF4
1.000 0.040 18 55431862 intron variant C/G;T snv 3
rs201203751
FYB1
0.925 0.040 5 39203496 intron variant TT/-;T;TTT delins 3
rs34177316
LOC107986273 ; APBB2
0.925 0.040 4 40985283 intron variant A/-;AA;AAA delins 3
rs3843954 1.000 0.040 13 57974377 intergenic variant G/A;C snv 3
rs599550
TCF4
1.000 0.040 18 55585157 intron variant G/A;T snv 3
rs6063349
CSE1L
0.925 0.040 20 49065345 intron variant G/A;C;T snv 3
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs7212450
LOC105371490
1.000 0.040 17 2688646 intron variant G/A;C snv 3
rs75995702 0.925 0.040 11 42785177 intergenic variant C/G;T snv 3
rs7939345 1.000 0.040 11 47959016 intergenic variant T/A;G snv 3
rs8100891 1.000 0.040 19 32338607 intergenic variant C/A;G snv 3
rs10156548 1.000 0.040 9 23318435 intron variant G/C;T snv 2
rs1055447
ARFGAP2 ; C11orf49
1.000 0.040 11 47164873 3 prime UTR variant C/A;T snv 2
rs11599236
SORCS3
1.000 0.040 10 104694914 intron variant T/C;G snv 2
rs11605020
LOC105369562
1.000 0.040 11 127110970 intron variant G/A;C snv 2
rs11693031
ERBB4
1.000 0.040 2 211813206 intron variant A/G;T snv 2
rs11826064 1.000 0.040 11 50818695 intergenic variant C/A;T snv 2
rs12030991 1.000 0.040 1 106683737 intergenic variant G/C;T snv 2
rs12938775
PAFAH1B1
1.000 0.040 17 2671527 intron variant G/A;T snv 2
rs13060816
BBX
1.000 0.040 3 107561639 intron variant T/A;C snv 2
rs1360380 1.000 0.040 9 23378490 intron variant G/A;T snv 2
rs1422192
LINC00461
1.000 0.040 5 88663205 intron variant G/A;T snv 2
rs1427027 1.000 0.040 18 37666359 intron variant C/G;T snv 2