Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31 15
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 15
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 11
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 9
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 9
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 8
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 7