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
rs41293463
BRCA1
0.790 0.280 17 43051071 missense variant A/C;T snv 1.2E-05 4
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 4
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 3
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 2
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs7073837
ARID5B
0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 1
rs3740390
AS3MT ; BORCS7-ASMT
0.925 0.080 10 102878723 intron variant C/T snv 9.2E-02 1
rs2234767
FAS ; ACTA2
0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 1
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 1