Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 11
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C 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
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 9
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 9
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 8
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6