Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11039149
NR1H3
0.827 0.280 11 47255124 intron variant A/G snv 0.19 6
rs1561927
LINC00824
0.807 0.280 8 128555832 intron variant C/T snv 0.65 6
rs2162679
IGF1
0.851 0.240 12 102477481 intron variant C/G;T snv 6
rs2206734
CDKAL1
0.882 0.160 6 20694653 intron variant C/T snv 0.20 6
rs2239186
VDR
0.882 0.120 12 47875627 intron variant A/C;G snv 0.17 5
rs10094872
CASC11
0.882 0.200 8 127707639 intron variant A/T snv 0.33 4
rs2941471
HNF4G
0.851 0.240 8 75558169 intron variant G/A snv 0.65 4
rs3790844
NR5A2
0.882 0.200 1 200038304 intron variant A/C;G snv 4
rs4759313
HOTAIR
0.851 0.120 12 53965290 intron variant T/A snv 0.51 4
rs7859034
SMC2
0.851 0.120 9 104103411 intron variant G/T snv 0.60 4
rs11141915
DAPK1
0.882 0.160 9 87620879 intron variant A/C snv 0.25 3
rs11644322
WWOX
0.925 0.120 16 79005703 intron variant C/T snv 0.22 3
rs1537373
CDKN2B-AS1
0.925 0.120 9 22103342 intron variant T/G snv 0.63 3
rs2001389
SUFU
0.925 0.120 10 102615501 intron variant G/A;C snv 3
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 3
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 3
rs10500715
SBF2
0.925 0.120 11 9951515 intron variant T/G snv 0.39 2
rs10835188
LIN7C
1.000 0.120 11 27501639 intron variant G/T snv 0.68 2
rs11085754
SMARCA4
0.925 0.120 19 11017920 intron variant A/G snv 0.41 2
rs11644043
BRD7
0.925 0.120 16 50327466 intron variant T/C snv 0.24 2
rs12362504
SBF2 ; LOC101928008
0.925 0.120 11 9907995 intron variant T/C snv 0.37 2
rs12456874
LDLRAD4
0.925 0.120 18 13366863 intron variant A/G snv 0.20 2
rs12939944
MAP2K4
0.925 0.120 17 12056502 intron variant C/T snv 0.45 2
rs13303010
KLHL17 ; NOC2L
0.925 0.120 1 959193 intron variant G/A snv 0.82 0.69 2
rs1630747
SLC5A3 ; MRPS6
0.925 0.120 21 34085692 intron variant C/A snv 0.69 2