Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs121908818
CIAO1 ; TMEM127
0.925 0.080 2 96265224 stop gained C/G;T snv 7.0E-06 1
rs36119840
GDNF-AS1 ; GDNF
0.807 0.280 5 37816010 missense variant G/A snv 2.3E-03 2.7E-03 3
rs201743423
MAX
1.000 0.040 14 65102315 missense variant C/A snv 8.9E-05 7.0E-05 1
rs149617956
MITF
0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 1
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 4
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
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
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 1
rs377767430
RET
0.882 0.080 10 43120192 missense variant A/C;G snv 1
rs75234356
RET
0.716 0.240 10 43120144 missense variant T/G snv 1.2E-05 7.0E-06 1
rs77558292
RET
0.776 0.160 10 43113621 missense variant T/A;C;G snv 1
rs78014899
RET
0.742 0.160 10 43118392 missense variant G/A;C;T snv 8.0E-06 1
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 1
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
rs121917755
SDHB
1.000 0.040 1 17028724 missense variant G/A;C snv 8.0E-06 1
rs138996609
SDHB
0.882 0.080 1 17022685 missense variant G/A snv 8.0E-06 7.0E-06 1
rs727504457
SDHB
0.925 0.080 1 17033086 missense variant A/G snv 1