Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 7
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 7
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 6
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 6
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv 6
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 6
rs806794
H2AC7 ; H3C4 ; H2BC7
6 26200449 3 prime UTR variant A/G snv 0.36 6
rs9292468 5 32818967 intergenic variant T/A;C snv 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28 5
rs2282978
LOC112268009 ; CDK6
7 92635096 intron variant T/C snv 0.38 5
rs2523578 1.000 6 31360765 upstream gene variant G/A snv 0.79 5
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs4896582
ADGRG6
6 142382740 intron variant G/A snv 0.50 5