Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9913911
GAS7
0.925 0.040 17 10127866 intron variant A/G snv 0.32 4
rs10038177
WDR36
0.925 0.040 5 111100751 intron variant C/T snv 0.53 0.54 3
rs12150284
GAS7
1.000 0.040 17 10127773 intron variant C/A;G;T snv 3
rs1579050
FMNL2
0.925 0.040 2 152508013 intron variant A/G snv 0.42 3
rs284489
ZFPM2
0.882 0.080 8 104945792 intron variant A/G snv 0.45 3
rs3766355
PTGFR
0.882 0.040 1 78491756 intron variant C/A;T snv 3
rs643319
CDKN2B-AS1
0.882 0.080 9 22017837 intron variant C/A snv 0.40 3
rs6475604
CDKN2B-AS1
0.925 0.040 9 22052735 intron variant T/C snv 0.72 3
rs6478746 0.925 0.040 9 126605119 intron variant G/A snv 0.72 3
rs690037
RFTN1 ; OXNAD1
0.882 0.040 3 16354161 intron variant C/G;T snv 3
rs750460
LOXL1
1.000 0.040 15 73949165 intron variant G/A;T snv 3
rs7854658
LMX1B
0.882 0.040 9 126652659 intron variant G/A snv 0.26 3
rs10918274
TMCO1
1.000 0.040 1 165745179 intron variant T/C snv 0.89 2
rs11217878
ARHGEF12
1.000 0.040 11 120469674 intron variant G/A snv 0.20 2
rs113985657
EXOC2
1.000 0.040 6 597203 intron variant C/T snv 0.14 2
rs12154178
ESR1
0.925 0.040 6 151929945 intron variant C/A snv 0.59 2
rs12377624
LOC105376277
1.000 0.040 9 126610831 intron variant G/C snv 0.28 2
rs12440667
LOXL1
1.000 0.040 15 73939098 intron variant C/A;T snv 2
rs12994401
LOC730100
0.925 0.040 2 51845108 intron variant C/T snv 0.18 2
rs13178997
WDR36
0.925 0.040 5 111108550 intron variant G/A;T snv 2
rs1992314
LOXL1
0.925 0.040 15 73931426 intron variant C/G snv 0.29 2
rs2028386
LOXL1
1.000 0.040 15 73934367 intron variant C/A;G snv 2
rs2073006
EXOC2
0.925 0.040 6 637465 intron variant C/T snv 0.11 2
rs28500712
AFAP1
1.000 0.040 4 7894486 intron variant A/C;G snv 2
rs28520091
AFAP1
1.000 0.040 4 7844513 intron variant C/A;G;T snv 2