Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 22
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs3750817
FGFR2
0.851 0.080 10 121573063 intron variant C/G;T snv 4
rs10500204
INSR
0.882 0.160 19 7182952 intron variant A/C snv 0.25 3
rs2382112 0.925 0.080 2 147841581 upstream gene variant G/A;C snv 2
rs12124649
MAST2
0.925 0.080 1 46033535 intron variant A/G;T snv 2