Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71 5
rs540730
R3HDM2
12 57413331 intron variant T/C snv 0.71 3
rs4017074 3 133541583 downstream gene variant T/C snv 0.71 1
rs10734252 1.000 0.080 11 17383292 non coding transcript exon variant G/A snv 0.71 3
rs2484294 10 114032303 intergenic variant G/A snv 0.70 4
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs56960668 8 143218568 downstream gene variant A/G snv 0.69 2
rs4953404 2 46659003 intergenic variant G/A snv 0.69 1
rs2896635
ARNTL
11 13338198 intron variant T/A snv 0.69 2
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 9
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs2972143 1.000 0.080 2 226251649 intergenic variant A/G snv 0.67 4
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs465002
C5orf67
5 56512648 intron variant C/T snv 0.67 3
rs6778062 3 133548309 upstream gene variant G/C snv 0.66 1
rs486142 1 234712862 non coding transcript exon variant G/A snv 0.65 2
rs4854727 3 133539041 downstream gene variant A/G snv 0.65 1
rs6785365 3 133543601 upstream gene variant A/G snv 0.65 1
rs4551304
PINX1
8 10807559 intron variant A/G snv 0.65 3
rs6439441
SRPRB
3 133810750 non coding transcript exon variant A/G snv 0.64 1
rs6439443
SRPRB
3 133822071 intron variant T/C snv 0.63 1
rs4277405 17 63471557 upstream gene variant C/T snv 0.63 4
rs2737216
TRPS1
8 115617852 intron variant A/T snv 0.62 2
rs57457691
PEPD
19 33420799 intron variant T/C snv 0.62 3