Source: ALL
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-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs2228224
GLI1
1.000 0.120 12 57471538 missense variant G/A snv 0.50 0.48 3
rs1131690998
PTCH1
0.925 0.280 9 95506484 missense variant A/C snv 2