Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28933981
TTR
0.807 0.200 18 31598647 missense variant C/T snv 1.5E-03 1.7E-03 8
rs121918027
PLG
0.827 0.320 6 160738593 missense variant G/A snv 1.4E-03 3.5E-04 7
rs121918095
TTR
0.827 0.160 18 31598602 missense variant G/A snv 7.9E-04 2.2E-04 6
rs12938
C1orf112 ; SELL
0.851 0.160 1 169691640 3 prime UTR variant A/G snv 0.27 5
rs267606743
COL4A1
1.000 0.160 13 110192222 missense variant C/T snv 5
rs1800458
TTR
0.851 0.280 18 31592902 missense variant G/A snv 5.1E-02 5.2E-02 5
rs755460305
KNG1
0.882 0.080 3 186732650 missense variant C/A snv 4
rs1967309
ADCY9
0.925 0.080 16 4015582 non coding transcript exon variant A/G snv 0.51 3
rs387906853
SMAD3
0.925 0.040 15 67181297 stop gained G/A;T snv 3
rs34203073
AGGF1
1.000 0.040 5 77035624 missense variant G/A snv 1.0E-02 9.9E-03 2
rs759985000
BDNF
11 27700987 5 prime UTR variant G/A;C snv 4.2E-06; 8.4E-06 2
rs6809699
P2RY12 ; MED12L
1.000 0.080 3 151338810 synonymous variant A/C snv 0.87 0.88 2
rs313158 6 85334045 intergenic variant A/T snv 1.8E-02 1
rs2144151
ANGPT4
20 903001 intron variant T/G snv 0.40 1
rs764821003
TGFBR2
3 30671823 missense variant G/A snv 1.4E-05 1