Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs377767430
RET
0.882 0.080 10 43120192 missense variant A/C;G snv 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 1
rs397516441
VHL
0.882 0.200 3 10149790 missense variant A/G snv 2
rs104894304
SDHD
0.827 0.240 11 112094831 missense variant A/G snv 1
rs121908827
TMEM127
1.000 0.040 2 96254107 missense variant A/G snv 1
rs267607170
VHL
0.882 0.200 3 10149814 missense variant A/G snv 1
rs727504457
SDHB
0.925 0.080 1 17033086 missense variant A/G snv 1
rs786202732
SDHB
0.882 0.080 1 17024041 missense variant A/G snv 1
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 4
rs104894302
SDHD
0.851 0.200 11 112089002 missense variant A/G;T snv 4.0E-06 1
rs876659329
SDHB
1.000 0.040 1 17044767 missense variant A/G;T snv 1
rs201743423
MAX
1.000 0.040 14 65102315 missense variant C/A snv 8.9E-05 7.0E-05 1
rs772551056
SDHB
0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 2
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
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 3
rs121908820
TMEM127 ; CIAO1
1.000 0.040 2 96265165 missense variant C/G snv 3.7E-05 3.5E-05 1
rs5030820
VHL
0.827 0.280 3 10149822 missense variant C/G;T snv 8.0E-06 2
rs121908818
CIAO1 ; TMEM127
0.925 0.080 2 96265224 stop gained C/G;T snv 7.0E-06 1
rs397516440
VHL
0.851 0.280 3 10142166 missense variant C/G;T snv 4.5E-06 1
rs74315368
SDHB
0.882 0.080 1 17022648 missense variant C/T snv 1.2E-05 1.4E-05 2
rs80338844
SDHD
0.776 0.280 11 112088939 missense variant C/T snv 2.0E-05 1.4E-05 2
rs121908819
TMEM127 ; CIAO1
1.000 0.040 2 96265174 missense variant C/T snv 2.0E-04 7.2E-04 1
rs121908823
TMEM127
1.000 0.040 2 96254974 missense variant C/T snv 6.7E-04 2.6E-03 1