Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554888939
EHMT1
0.683 0.640 9 137798823 missense variant G/T snv 58
rs121918459
PTPN11
0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 46
rs727502818
KCNC1
0.790 0.160 11 17772053 missense variant G/A snv 20
rs11031006
LOC105376607
0.882 0.120 11 30204981 intron variant G/A snv 0.11 7
rs16991615
MCM8
0.925 0.080 20 5967581 missense variant G/A snv 4.5E-02 4.2E-02 6
rs72709458
TERT
0.882 0.040 5 1283640 intron variant C/A;T snv 5