Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 18
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 11
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 10
rs104893824
VHL
0.776 0.320 3 10142181 missense variant T/A;C snv 7
rs5030805
VHL
0.790 0.280 3 10142086 missense variant G/A;T snv 7
rs377767404
RET
0.742 0.160 10 43114488 missense variant T/C snv 6
rs77558292
RET
0.776 0.160 10 43113621 missense variant T/A;C;G snv 6
rs1183365192
RET
0.851 0.160 10 43106550 missense variant C/T snv 7.0E-06 4
rs1188254133
VEGFA
0.851 0.240 6 43781990 missense variant T/G snv 7.0E-06 4
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 4
rs1420960657
SDHD
0.851 0.080 11 112093192 missense variant A/G snv 4
rs1400537035
SERPINE1
0.882 0.200 7 101131931 missense variant C/A;G;T snv 3
rs377767405
RET
0.827 0.120 10 43114489 missense variant G/A;C;T snv 3
rs869025648
VHL
0.851 0.240 3 10146587 synonymous variant A/G snv 3
rs267607170
VHL
0.882 0.200 3 10149814 missense variant A/G snv 2
rs377767430
RET
0.882 0.080 10 43120192 missense variant A/C;G snv 2
rs79661516
RET
0.882 0.080 10 43105018 missense variant G/A snv 2
rs869025630
VHL
0.925 0.080 3 10142158 missense variant G/C;T snv 2
rs876659313
VHL
0.925 0.080 3 10146624 missense variant A/C;G snv 2
rs74799832
RET
0.662 0.280 10 43121968 missense variant T/C snv 4.0E-06 21
rs397516444
VHL
0.882 0.200 3 10149808 missense variant G/A;T snv 4.0E-06 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 17
rs1060503770
SDHD
0.851 0.200 11 112094815 stop gained C/G;T snv 4.0E-06 3