Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10097505
ARC
0.925 0.120 8 142612823 3 prime UTR variant G/A snv 0.47 2
rs10163755
DSG4 ; DSG1-AS1
0.827 0.200 18 31405413 intron variant G/A snv 0.74 6
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104894664
TTR
0.882 0.120 18 31592959 missense variant G/A snv 6
rs104894665
TTR
0.851 0.120 18 31593017 missense variant T/C snv 5
rs104895219
TNFRSF1A
0.827 0.240 12 6333823 missense variant G/A;T snv 5
rs11541796
TTR
0.807 0.280 18 31593011 missense variant A/G snv 9
rs1217777010
APOA1-AS ; APOA1
1.000 0.040 11 116836182 missense variant C/T snv 4.0E-06 1
rs121909211
TGFBI
0.724 0.200 5 136046407 missense variant G/A;T snv 4.0E-05 15
rs121909612
FGA
0.807 0.160 4 154585795 missense variant T/A snv 4.0E-06 7.0E-06 6
rs121909715
GSN
0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 8
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs121913547
LYZ
0.807 0.200 12 69350192 missense variant T/C snv 7
rs121913549
LYZ
0.882 0.200 12 69350194 missense variant T/A snv 3
rs121918068
TTR
0.882 0.200 18 31592983 missense variant T/A;C snv 6
rs121918074
TTR
0.851 0.120 18 31595247 missense variant C/A snv 6.0E-04 3.9E-04 5
rs121918075
TTR
0.752 0.280 18 31598632 missense variant A/G snv 15
rs121918077
TTR
0.882 0.120 18 31592992 missense variant G/C snv 3
rs121918079
TTR
0.790 0.280 18 31595143 missense variant T/C snv 10
rs121918082
TTR
0.827 0.280 18 31595244 missense variant G/C snv 6
rs121918088
TTR
0.851 0.120 18 31598631 missense variant T/C snv 4
rs121918094
TTR
0.827 0.280 18 31592921 missense variant T/C snv 8
rs121918095
TTR
0.827 0.160 18 31598602 missense variant G/A snv 7.9E-04 2.2E-04 6
rs121918097
TTR
0.790 0.280 18 31595137 missense variant G/A snv 10
rs121918098
TTR
0.807 0.200 18 31592939 missense variant A/G snv 7