Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1772578 1.000 0.080 13 80614113 downstream gene variant A/G snv 0.55 2
rs73568641 1.000 0.080 6 153704004 intergenic variant T/C snv 0.14 2
rs9360217 1.000 0.080 6 66628700 intergenic variant T/G snv 0.21 2
rs10799590
CNIH3
1 224634780 intron variant G/A snv 0.56 2
rs7578347
LOC100506474
1.000 0.080 2 12981042 non coding transcript exon variant C/T snv 0.24 2
rs12442183
LOC105370980
1.000 0.080 15 93204756 intergenic variant C/T snv 0.38 2
rs12104412
ZNF565
1.000 0.080 19 36240156 intron variant A/G;T snv 4.2E-02 2
rs10738186 9 10753414 intergenic variant G/A snv 0.80 1
rs10995853 10 64259979 intron variant C/G snv 3.3E-02 1
rs13097862 3 63733563 intergenic variant A/C;G;T snv 1
rs1872052 15 93209649 intergenic variant T/C snv 0.44 1
rs4300379 11 54614287 intergenic variant C/T snv 0.57 1
rs8036747 15 93209226 intergenic variant G/A snv 0.47 1
rs11163319
ADGRL2
1 81506757 intron variant A/C snv 9.9E-02 1
rs13279512
CLVS1
8 61045943 intergenic variant G/A snv 0.24 1
rs74641711
CTDP1
18 79727394 intron variant C/T snv 1.6E-02 1
rs1557219
LOC101927293
6 58044647 intron variant C/T snv 0.69 1
rs1970606
LOC101927293
6 58042294 intron variant G/A snv 0.70 1
rs17300532
LOC105379028
5 72084528 downstream gene variant C/T snv 1
rs192590503
NKAIN2
6 124215869 intron variant G/A snv 2.0E-02 1
rs58356853
TACC2
10 122011617 intron variant C/T snv 9.7E-02 1
rs59675243
TACC2
10 122011107 intron variant C/A snv 9.7E-02 1
rs75449825
TACC2
10 122010374 intron variant C/A;G snv 9.7E-02 1