Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74315367
SDHB
0.882 0.080 1 17024025 missense variant G/C snv 4.0E-06 1
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
rs786202732
SDHB
0.882 0.080 1 17024041 missense variant A/G snv 1
rs876658367
SDHB
0.882 0.080 1 17024028 missense variant C/T snv 1
rs876659329
SDHB
1.000 0.040 1 17044767 missense variant A/G;T snv 1
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
rs104894302
SDHD
0.851 0.200 11 112089002 missense variant A/G;T snv 4.0E-06 1
rs104894304
SDHD
0.827 0.240 11 112094831 missense variant A/G snv 1
rs121908819
TMEM127 ; CIAO1
1.000 0.040 2 96265174 missense variant C/T snv 2.0E-04 7.2E-04 1
rs121908820
TMEM127 ; CIAO1
1.000 0.040 2 96265165 missense variant C/G snv 3.7E-05 3.5E-05 1
rs121908823
TMEM127
1.000 0.040 2 96254974 missense variant C/T snv 6.7E-04 2.6E-03 1
rs121908824
TMEM127
1.000 0.040 2 96254962 missense variant G/A;C;T snv 2.0E-05; 4.0E-06 1
rs121908827
TMEM127
1.000 0.040 2 96254107 missense variant A/G snv 1
rs121908828
TMEM127
1.000 0.040 2 96254106 missense variant C/A;T snv 4.0E-06 1
rs5030824
VHL
0.776 0.320 3 10149885 missense variant C/G snv 2.0E-05 4.2E-05 3
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