Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11230661
OR4P1P
11 55683837 non coding transcript exon variant G/A snv 0.14 2
rs11246533 11 54742025 intergenic variant G/A snv 0.11 2
rs112640876
LSP1
11 1873813 intron variant A/G;T snv 3
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs113862204
CACNB2
10 18396076 intron variant C/T snv 0.29 2
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs115714636
ITIH3
3 52796511 missense variant A/G snv 1.6E-03 6.4E-03 1
rs11576729
PGM1
1 63648758 intron variant G/A;T snv 1
rs115888294 8 94105161 upstream gene variant T/C snv 2.4E-02 1
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs11681792
NRXN1
1.000 0.080 2 49957256 intron variant C/T snv 0.12 4
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs117222687
COMT ; ARVCF
22 19968491 intron variant G/C snv 3.8E-02 4.1E-02 2
rs11725969
GUCY1A1
4 155705436 intron variant C/T snv 0.24 5
rs11731886
LOC105377506
4 155738667 downstream gene variant A/C snv 0.21 3
rs11756347 6 126856325 intron variant A/G snv 0.36 2
rs11762784
LOC105375508
7 130739885 intergenic variant G/A snv 0.38 3
rs11766519 7 57524150 intergenic variant T/C snv 0.13 1
rs117753190
ABCA6
17 69140184 intron variant C/G snv 2.0E-02 2
rs11781008 8 9295729 intron variant G/C;T snv 2
rs11786677
MSRA
8 10406750 intron variant A/G snv 0.46 2
rs11870935
KPNB1
17 47655239 intron variant G/A;C snv 4