Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 18
rs2280401
SNORD35B ; RPS11
19 49496752 intron variant G/A snv 0.12 5
rs694419 18 62458879 regulatory region variant T/C snv 0.53 2
rs16948098
FRMD5
15 43927409 intron variant G/A snv 9.5E-02 2
rs11671010
HPN-AS1
19 35068570 intron variant T/C snv 0.11 2
rs4806073
HPN-AS1 ; HPN
19 35064286 intron variant T/C snv 0.85 2
rs2293579
PSMC3
11 47419207 intron variant G/A snv 0.35 0.30 2
rs11078597
WDR81 ; MIR22HG ; MIR22
17 1715069 intron variant T/C snv 0.19 2