Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800038
ADRA2A
10 111079134 synonymous variant C/A snv 7.4E-02 4.9E-02 1
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs201607471
ADRB3
8 37966397 missense variant C/T snv 8.5E-06 1
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 5
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 4
rs945508
ARHGEF11 ; MIR765 ; LRRC71
1.000 0.080 1 156937289 missense variant T/C snv 0.64 0.66 3
rs3792267
CAPN10
0.882 0.200 2 240591757 non coding transcript exon variant G/A snv 0.23 4
rs2975760
CAPN10
1.000 0.080 2 240591746 non coding transcript exon variant T/C snv 0.12 3
rs5030952
CAPN10
0.925 0.160 2 240603286 intron variant C/G;T snv 3
rs4586
CCL2
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48 8
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 9
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs9465871
CDKAL1
0.882 0.120 6 20717024 intron variant T/C snv 0.30 4
rs6456368
CDKAL1
1.000 0.080 6 20659575 intron variant T/C snv 0.40 2
rs6935599
CDKAL1
1.000 0.080 6 20716864 intron variant A/G snv 0.31 2
rs7747752
CDKAL1
1.000 0.080 6 20725192 intron variant G/C snv 0.34 2
rs7767391
CDKAL1
1.000 0.080 6 20725009 intron variant T/C snv 0.28 2
rs9348440
CDKAL1
1.000 0.080 6 20641105 intron variant C/T snv 0.13 2
rs9350276
CDKAL1
1.000 0.080 6 20740065 intron variant C/T snv 0.38 2
rs2328549
CDKAL1
6 20718009 intron variant A/T snv 0.18 1