Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2178146 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 5
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 2
rs11869286
STARD3
0.925 0.080 17 39657603 intron variant G/C snv 0.52 2
rs2070803
TRIM46
0.925 0.080 1 155185239 intron variant G/A snv 0.55 2
rs6733301
EFR3B
0.925 0.080 2 25053415 intron variant G/A snv 0.13 2
rs881844
STARD3
0.925 0.080 17 39653965 intron variant C/G snv 0.51 2
rs9471643
PGC
0.882 0.080 6 41751177 intron variant G/C snv 0.19 2
rs9972882
STARD3
0.925 0.080 17 39651445 intron variant A/C snv 0.66 2
rs11187842
PLCE1
0.925 0.080 10 94292754 intron variant C/T snv 7.8E-02 1
rs1135354
IL18R1
0.925 0.080 2 102397842 3 prime UTR variant T/G snv 0.23 1
rs12155758 0.882 0.080 8 142684467 upstream gene variant G/A snv 0.23 1
rs1371429276
PTPRT
1.000 0.080 20 42472359 missense variant G/A snv 1.4E-05 1
rs17033
ADH1B
0.925 0.080 4 99307788 3 prime UTR variant T/C snv 9.6E-02 1
rs2515401
IL36RN
0.882 0.080 2 113062899 3 prime UTR variant T/A;C snv 1
rs3180235
IL36RN
0.882 0.080 2 113063095 3 prime UTR variant A/G snv 0.65 1
rs3761376
TFF1
0.925 0.080 21 42366929 upstream gene variant G/A snv 0.27 1
rs4460629 0.882 0.080 1 155162859 intergenic variant T/C snv 0.56 1
rs526934
TCN1
0.925 0.080 11 59866020 intron variant G/A snv 0.77 1
rs63749803
MLH1
1.000 0.080 3 37004421 missense variant T/C;G snv 1
rs63750297
MLH1
1.000 0.080 3 37004412 missense variant C/A;G;T snv 8.0E-06 1
rs63750795
MSH2
1.000 0.080 2 47480854 missense variant T/G snv 1
rs63750966
MSH2
1.000 0.080 2 47403240 missense variant G/A;C;T snv 1
rs63751047
MLH1
1.000 0.080 3 37048525 missense variant C/A;G snv 1
rs63751400
MSH2
1.000 0.080 2 47480839 missense variant C/G;T snv 4.0E-06 1
rs753724
PLCE1
0.882 0.080 10 94291660 intron variant G/A;C;T snv 1