Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs10750766 11 65706327 regulatory region variant C/A snv 0.60 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
rs11870935
KPNB1
17 47655239 intron variant G/A;C snv 4
rs11967262 6 43792590 intergenic variant C/G snv 0.41 4
rs1275984 2 26688641 upstream gene variant A/C;G 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
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs2484294 10 114032303 intergenic variant G/A snv 0.70 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
rs41274050
ASAH2B ; A1CF
10 50814012 missense variant C/A;T snv 4.0E-06; 5.3E-03 4