Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 4
rs36119840
GDNF-AS1 ; GDNF
0.807 0.280 5 37816010 missense variant G/A snv 2.3E-03 2.7E-03 3
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 3
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
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 3
rs77939446
RET
0.724 0.120 10 43113622 missense variant G/A;C;T snv 4.0E-06 3
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 3
rs5030824
VHL
0.776 0.320 3 10149885 missense variant C/G snv 2.0E-05 4.2E-05 3
rs377767405
RET
0.827 0.120 10 43114489 missense variant G/A;C;T snv 2
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 2
rs74315368
SDHB
0.882 0.080 1 17022648 missense variant C/T snv 1.2E-05 1.4E-05 2
rs772551056
SDHB
0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 2
rs80338844
SDHD
0.776 0.280 11 112088939 missense variant C/T snv 2.0E-05 1.4E-05 2
rs80338845
SDHD
0.807 0.240 11 112088971 missense variant G/T snv 7.0E-06 2
rs1553619948
VHL
0.882 0.200 3 10146528 missense variant T/C snv 2
rs397516441
VHL
0.882 0.200 3 10149790 missense variant A/G snv 2
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
rs5030833
VHL
0.925 0.160 3 10146580 missense variant T/C;G snv 4.0E-06 2
rs730882035
VHL
0.807 0.200 3 10149805 missense variant G/A snv 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1