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
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs2234767
FAS ; ACTA2
0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs13405728
STON1-GTF2A1L ; LHCGR
0.790 0.200 2 48751020 intron variant A/G snv 0.15 8
rs2059807
INSR
0.851 0.200 19 7166098 intron variant A/G;T snv 7
rs4385527
AOPEP
0.827 0.280 9 94886305 intron variant G/A snv 0.31 6
rs10818854
DENND1A
0.851 0.200 9 123684499 intron variant G/A snv 5.7E-02 6
rs1057518903
MEN1
0.882 0.160 11 64807890 splice region variant C/- delins 6
rs13429458
THADA
0.827 0.200 2 43411699 intron variant A/C snv 0.14 6
rs12478601
THADA
0.851 0.200 2 43494369 intron variant C/T snv 0.61 5
rs17759659
BCL2
0.851 0.120 18 63291411 intron variant A/G snv 0.31 4