Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs223331
CISD2
0.851 0.160 4 102872408 intron variant T/A;C snv 5
rs223330
CISD2
0.851 0.160 4 102872502 intron variant T/A;C snv 4
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs72783884
PAM
1.000 0.080 5 102912212 intron variant A/T snv 6.8E-03 1
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs78408340
PAM
1.000 0.080 5 103003035 missense variant C/G;T snv 3.7E-03; 8.1E-06 2
rs35658696
PAM
1.000 0.080 5 103003107 missense variant A/G snv 3.1E-02 3.2E-02 3
rs7674212
SLC9B2
1.000 0.080 4 103067742 intron variant G/A;T snv 1
rs115505614
GIN1
1.000 0.080 5 103087264 3 prime UTR variant C/T snv 3.2E-02 1
rs75432112 1.000 0.080 5 103250706 intron variant G/A snv 3.0E-02 1
rs1384401
TACR3
1.000 0.080 4 103643921 intron variant G/A snv 0.44 1
rs2299383
RELN
1.000 0.080 7 103778399 intron variant C/T snv 0.41 2
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 3
rs649891
PTPRD
1.000 0.080 9 10430602 intron variant T/A;C snv 1
rs13268287
LRP12
1.000 0.080 8 104548593 intron variant A/G snv 1.6E-02 1
rs10515353 1.000 0.080 5 104585969 intron variant T/C snv 0.14 1
rs3803304
AKT1
0.882 0.160 14 104772809 intron variant C/G snv 0.24 3
rs2494738
AKT1
1.000 0.080 14 104780349 intron variant G/A snv 1.0E-01 1
rs2494746
AKT1
1.000 0.080 14 104791382 intron variant C/G snv 0.77 1
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs2498786
AKT1
0.925 0.160 14 104796031 upstream gene variant C/G snv 0.50 2
rs2230808
ABCA1
0.827 0.240 9 104800523 missense variant T/C snv 0.71 0.60 6
rs12582312
SLC41A2
1.000 0.080 12 104821402 intron variant C/T snv 2.4E-02 1
rs10861279
SLC41A2
1.000 0.080 12 104821412 intron variant A/C;G snv 1
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13