Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs749437638
ARVCF ; COMT
0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs28933981
TTR
0.807 0.200 18 31598647 missense variant C/T snv 1.5E-03 1.7E-03 8
rs763000109
TNF
0.827 0.240 6 31575788 missense variant C/G;T snv 4.1E-06; 1.6E-05 9
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
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
rs267606743
COL4A1
1.000 0.160 13 110192222 missense variant C/T snv 5
rs34203073
AGGF1
1.000 0.040 5 77035624 missense variant G/A snv 1.0E-02 9.9E-03 2
rs6809699
P2RY12 ; MED12L
1.000 0.080 3 151338810 synonymous variant A/C snv 0.87 0.88 2