Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 3
rs121908828
TMEM127
1.000 0.040 2 96254106 missense variant C/A;T snv 4.0E-06 1
rs74315367
SDHB
0.882 0.080 1 17024025 missense variant G/C snv 4.0E-06 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs772551056
SDHB
0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 2
rs5030821
VHL
0.827 0.280 3 10149823 missense variant G/A;C;T snv 4.0E-06 2
rs397516444
VHL
0.882 0.200 3 10149808 missense variant G/A;T snv 4.0E-06 1
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 2
rs104894302
SDHD
0.851 0.200 11 112089002 missense variant A/G;T snv 4.0E-06 1
rs5030833
VHL
0.925 0.160 3 10146580 missense variant T/C;G snv 4.0E-06 2
rs1060503555
VHL
1.000 0.040 3 10146613 missense variant T/C snv 4.0E-06 7.0E-06 1
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 3
rs1553619948
VHL
0.882 0.200 3 10146528 missense variant T/C snv 2
rs377767405
RET
0.827 0.120 10 43114489 missense variant G/A;C;T 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
rs730882035
VHL
0.807 0.200 3 10149805 missense variant G/A snv 2
rs80338845
SDHD
0.807 0.240 11 112088971 missense variant G/T snv 7.0E-06 2
rs104893824
VHL
0.776 0.320 3 10142181 missense variant T/A;C snv 1
rs104893826
VHL
0.882 0.200 3 10142038 missense variant G/A;C snv 1
rs104893827
VHL
1.000 0.040 3 10142035 missense variant T/A;C snv 1
rs104894304
SDHD
0.827 0.240 11 112094831 missense variant A/G snv 1
rs121908818
CIAO1 ; TMEM127
0.925 0.080 2 96265224 stop gained C/G;T snv 7.0E-06 1