Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912677
LOC101928174 ; ACTC1
1.000 0.080 15 34793326 missense variant T/C snv 2
rs121912683
SLC25A4
0.851 0.200 4 185145020 missense variant C/A snv 4.0E-06 7.0E-06 9
rs121912998
DSP ; LOC101928076
1.000 0.040 6 7542003 missense variant G/A snv 1.6E-03 1.1E-03 3
rs121913002
DES
0.851 0.160 2 219425727 missense variant C/A;G;T snv 6.5E-05; 5.6E-04 7
rs121913628
MYH7
0.763 0.160 14 23424059 missense variant C/G;T snv 10
rs121917776
VCL
0.882 0.040 10 74112086 missense variant C/T snv 9.9E-05 7.0E-06 5
rs121918070
TTR
1.000 0.120 18 31595157 missense variant A/G snv 4.0E-06 1.4E-05 2
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
rs121918086
TTR
1.000 0.120 18 31595160 missense variant G/A snv 3
rs121918090
TTR
0.790 0.240 18 31593026 missense variant G/C snv 8
rs121918093
TTR
0.882 0.200 18 31592944 missense variant G/A;C snv 4.0E-06 4
rs121918097
TTR
0.790 0.280 18 31595137 missense variant G/A snv 10
rs121918100
TTR
0.827 0.160 18 31595184 missense variant T/C snv 11
rs121918312
BAG3
0.776 0.160 10 119672373 missense variant C/A;T snv 11
rs121964856
TNNT2
0.807 0.120 1 201365297 missense variant C/A;T snv 8
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs1242465339
UQCRFS1
1.000 0.080 19 29207763 stop gained G/A;T snv 7.0E-06 3
rs12582717
SLCO1B1
12 21143872 intron variant C/G snv 4.1E-02 1
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1286964261
EIF1AD ; BANF1
11 66003356 missense variant G/A snv 7.0E-06 1
rs1334828551
MUL1
1 20500800 missense variant A/G snv 4.0E-06 1.4E-05 2
rs1343372308
MYH7 ; MHRT
14 23413792 missense variant C/G snv 7.0E-06 2
rs137854607
SCN5A
0.882 0.120 3 38554309 missense variant C/G;T snv 5
rs138119149
AARS2 ; TMEM151B
0.807 0.280 6 44304512 missense variant G/A snv 2.1E-04 2.4E-04 11