Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397516440
VHL
0.851 0.280 3 10142166 missense variant C/G;T snv 4.5E-06 1
rs397516441
VHL
0.882 0.200 3 10149790 missense variant A/G snv 2
rs397516444
VHL
0.882 0.200 3 10149808 missense variant G/A;T snv 4.0E-06 1
rs5030805
VHL
0.790 0.280 3 10142086 missense variant G/A;T snv 2
rs5030808
VHL
0.882 0.200 3 10142124 missense variant G/A;C;T snv 4.5E-06 2
rs5030809
VHL
0.776 0.320 3 10142139 missense variant T/C snv 1.3E-05 2
rs5030820
VHL
0.827 0.280 3 10149822 missense variant C/G;T snv 8.0E-06 2
rs5030821
VHL
0.827 0.280 3 10149823 missense variant G/A;C;T snv 4.0E-06 2
rs5030824
VHL
0.776 0.320 3 10149885 missense variant C/G snv 2.0E-05 4.2E-05 3
rs5030827
VHL
0.882 0.200 3 10142097 missense variant G/A;C;T snv 4.4E-06 1
rs5030833
VHL
0.925 0.160 3 10146580 missense variant T/C;G snv 4.0E-06 2
rs727504457
SDHB
0.925 0.080 1 17033086 missense variant A/G snv 1
rs730882035
VHL
0.807 0.200 3 10149805 missense variant G/A snv 2
rs74315367
SDHB
0.882 0.080 1 17024025 missense variant G/C snv 4.0E-06 1
rs74315368
SDHB
0.882 0.080 1 17022648 missense variant C/T snv 1.2E-05 1.4E-05 2
rs74315370
SDHB
0.882 0.080 1 17044825 stop gained G/A;C snv 1.6E-05 1
rs74315371
SDHB
1.000 0.040 1 17028721 missense variant C/T snv 1
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 2
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 3
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 1
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 3
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 3
rs772551056
SDHB
0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 2
rs77558292
RET
0.776 0.160 10 43113621 missense variant T/A;C;G snv 1
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 3