Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750447
MLH1
0.716 0.200 3 37025749 missense variant T/A snv 2.7E-03 7.5E-04 17
rs121913471
MIR4728 ; ERBB2
0.807 0.120 17 39724747 missense variant G/A;C;T snv 8
rs35054928
FGFR2
0.851 0.080 10 121580918 intron variant C/- delins 4
rs4593472
LINC-PINT
0.882 0.080 7 130982362 intron variant C/T snv 0.31 3
rs16886448
MAP3K1
0.882 0.080 5 56874986 intron variant C/G snv 6.6E-02 5.8E-02 3
rs3116068
BRMS1 ; RIN1
1.000 11 66337522 3 prime UTR variant C/T snv 0.17 2
rs1052566
RIN1 ; BRMS1
1.000 11 66337723 missense variant G/A snv 0.30 0.23 1