Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137853092
WNK4
0.851 0.240 17 42787494 missense variant C/G snv 5
rs188286943
VPS35
0.776 0.160 16 46662452 missense variant C/T snv 9
rs770029606
VPS35
1.000 16 46674629 missense variant G/A snv 7.7E-05 9.2E-05 1
rs74315431
VAPB
0.732 0.080 20 58418318 missense variant C/T snv 4.0E-06 15
rs74452732
UBA6-AS1 ; GNRHR
0.851 0.160 4 67753825 missense variant C/A;T snv 4.0E-06 4
rs1048103951
TXNRD1
0.925 0.040 12 104321282 missense variant G/A snv 2
rs587776983
TUBB4A
0.807 0.240 19 6502209 missense variant G/A;C;T snv 9
rs587777074
TUBB4A
0.790 0.240 19 6495688 missense variant C/T snv 4.0E-06 7
rs267607165
TUBB3
0.708 0.520 16 89935679 missense variant G/A;C snv 18
rs781587642
TUBA4A ; STK16
0.851 0.120 2 219250557 missense variant G/A;C snv 2.0E-05 6
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs121918075
TTR
0.752 0.280 18 31598632 missense variant A/G snv 15
rs121918098
TTR
0.807 0.200 18 31592939 missense variant A/G snv 7
rs121918095
TTR
0.827 0.160 18 31598602 missense variant G/A snv 7.9E-04 2.2E-04 6
rs121918077
TTR
0.882 0.120 18 31592992 missense variant G/C snv 3
rs138065384
TTR
0.925 0.040 18 31593016 missense variant T/C snv 4.4E-05 1.9E-04 3
rs121908873
TSHR ; LOC101928462
0.790 0.160 14 81139828 missense variant G/A;T snv 7
rs121908880
TSHR ; LOC101928462
0.882 0.040 14 81143973 missense variant C/T snv 3
rs199476301
TPM1
0.851 0.040 15 63042874 missense variant G/A;T snv 4.0E-06 6
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs1199893366
TP53
0.925 0.080 17 7674968 missense variant A/G snv 2
rs1057519980
TP53
1.000 17 7675084 missense variant G/C snv 1
rs4149584
TNFRSF1A
0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 24