Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs180177035
BRAF
0.752 0.280 7 140801502 missense variant T/C snv 35
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 32
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 16
rs727503109
KRAS
0.752 0.320 12 25245277 missense variant T/C snv 16
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs104894360
KRAS
0.724 0.560 12 25209904 missense variant T/A;C snv 14
rs397507483
BRAF
0.790 0.400 7 140753348 missense variant C/A;T snv 13
rs180177039
BRAF
0.851 0.160 7 140778006 missense variant T/A;C;G snv 12
rs397507478
BRAF
0.790 0.440 7 140777014 missense variant C/A snv 12
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 11
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs180177040
BRAF
0.790 0.360 7 140754187 missense variant T/C;G snv 9
rs104894366
KRAS
0.776 0.400 12 25245284 missense variant G/A;C snv 9
rs869025608
MAP2K1
0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 8
rs121908595
MAP2K1
0.827 0.280 15 66436843 missense variant A/G snv 4.0E-06 8
rs180177042
BRAF
0.807 0.280 7 140749365 missense variant A/C;T snv 7
rs387906660
BRAF
0.790 0.280 7 140801550 missense variant G/A;C;T snv 7
rs121908596
MAP2K1
0.807 0.240 15 66436837 missense variant G/A;T snv 7
rs121913378
BRAF
0.776 0.280 7 140753337 missense variant C/A;G;T snv 6
rs387906661
BRAF
0.807 0.280 7 140801551 missense variant T/G snv 6
rs397507466
BRAF
0.807 0.280 7 140801537 missense variant T/A;C;G snv 4.0E-06 6
rs397516792
MAP2K1
0.827 0.280 15 66436825 missense variant C/A;G;T snv 6