Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7096937
GPAM
10 112190660 intron variant T/C snv 0.72 5
rs7125196
LOC105369329
11 61505093 intron variant T/C snv 0.16 5
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 5
rs7570971
RAB3GAP1
1.000 0.080 2 135080336 intron variant C/A snv 0.61 5
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71 5
rs8177240
TF
3 133758857 intron variant T/C;G snv 0.29 5
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs10769254
MYBPC3
11 47340914 intron variant G/C snv 0.27 4
rs11105352
ATP2B1
12 89632685 intron variant G/A snv 0.14 4
rs111478946
ATP2B1
12 89665065 intron variant G/A snv 0.14 4
rs11681792
NRXN1
1.000 0.080 2 49957256 intron variant C/T snv 0.12 4
rs11870935
KPNB1
17 47655239 intron variant G/A;C snv 4
rs13135092
SLC39A8
4 102276925 intron variant A/G snv 5.1E-02 4
rs145485557
POC1B
12 89445110 intron variant C/T snv 4.7E-02 4
rs150844304
TP53BP1
15 43434427 intron variant A/C;G snv 4
rs1689040 12 89584456 intron variant C/G;T snv 4
rs1731243
KCNK3
2 26707543 intron variant C/T snv 0.48 4
rs17613287
CACNB2
10 18430748 intron variant A/T snv 0.27 4
rs2013208
RBM5 ; RBM6
3 50091966 intron variant C/T snv 0.61 0.56 4
rs2071449
HOXC4 ; HOXC5 ; MIR615
12 54034227 intron variant C/A;T snv 0.35; 4.2E-06 4
rs2586886
KCNK3
1.000 0.080 2 26709163 intron variant C/G;T snv 4
rs2749008
GSTA2
6 52761322 intron variant C/T snv 0.75 4
rs2999159
MOV10
1 112688136 intron variant A/G snv 0.85 4
rs34071855
CASZ1
1 10738432 intron variant C/G;T snv 4
rs3794695
HPR ; TXNL4B
16 72063928 intron variant C/A;T snv 4