Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs886037834
PKD1L1
0.827 0.160 7 47846960 missense variant C/G snv 7.0E-06 6
rs16899974
AGXT2
0.827 0.120 5 34998772 missense variant C/A snv 0.24 0.19 5
rs1273246817
RYR2
0.882 0.080 1 237784169 missense variant A/C snv 3
rs372827955
TBX5
1.000 0.080 12 114356026 missense variant G/A snv 4.4E-05 2.8E-05 2
rs1011490341
KCND2
1.000 0.080 7 120741596 missense variant C/A snv 4.0E-06 1.4E-05 1