Source: CURATED ×
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 22
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 14
rs80358721
BRCA2
0.724 0.320 13 32339320 stop gained C/A;G;R snv 4.2E-06 11
rs185229225
BOD1L1
0.851 0.120 4 13607505 intron variant T/C snv 4
rs121913322
STK11
0.882 0.120 19 1221320 missense variant C/A;G;T snv 2.9E-05; 1.2E-04 4
rs121964872
CDH1
0.882 0.120 16 68833362 missense variant A/G snv 4.4E-05 1.1E-04 3
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 1
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1