Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs661348
LSP1
11 1884062 intron variant T/C snv 0.43 0.37 5
rs10776752
WNT2B
1 112501706 intron variant G/T snv 8.8E-02 4
rs10948071
ZNF318
6 43312975 intron variant C/T snv 0.46 4
rs11105364
ATP2B1
12 89675499 intron variant T/G snv 0.15 4
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02 4
rs12129649
MOV10
1 112688881 5 prime UTR variant G/T snv 6.6E-02 4
rs12630213
FGD5
3 14912904 intron variant C/T snv 0.68 4
rs1401982
ATP2B1
12 89595822 intron variant G/A snv 0.60 4
rs1563788
ZNF318
6 43340625 intron variant C/T snv 0.42 4
rs17004869
FGF5
4 80283879 intron variant A/T snv 4.6E-02 4
rs1731243
KCNK3
2 26707543 intron variant C/T snv 0.48 4
rs1902859 4 80236549 regulatory region variant T/C snv 0.27 4
rs2240736
TBX2
17 61408032 non coding transcript exon variant C/T snv 0.64 0.68 4
rs2270860
SLC22A7 ; CRIP3
6 43302413 splice region variant C/T snv 0.37 0.43 4
rs2493134
AGT
1 230713613 intron variant T/C snv 0.57 4
rs2649044
SWAP70
11 9742422 intron variant C/T snv 0.55 4
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 4
rs35021474
KCNK3
2 26693976 intron variant C/G snv 0.48 4
rs3774427
CACNA1D
3 53531601 intron variant C/G snv 0.11 4
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 4
rs4684242
FGD5
3 14853598 intron variant G/C snv 0.20 4
rs4722675
HOTTIP
7 27204343 intron variant A/G snv 0.93 4
rs4910498
SWAP70
11 9743956 intron variant A/T snv 0.61 4
rs62524579 8 142979538 downstream gene variant G/A;C;T snv 4
rs62525059
GML
8 142901545 intron variant G/A snv 0.34 4