Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs162171
CEP128
14 80794033 intron variant A/C snv 0.64 1
rs17111237
CEP128
14 80939997 intron variant A/G snv 0.15 1
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 5
rs1057519901
FGFR2
0.925 0.080 10 121498525 missense variant T/G snv 5
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv 5
rs6498114
CIITA ; LOC105371080
1.000 0.080 16 10870261 intron variant G/T snv 0.78 2
rs1572072 1.000 0.120 13 23553071 intergenic variant G/T snv 0.36 2
rs189897
ITGA9
1.000 0.120 3 37477054 intron variant T/A snv 0.13 2
rs2517713
HLA-A
1.000 0.120 6 29950322 downstream gene variant G/A;T snv 2
rs28421666 1.000 0.120 6 32624960 upstream gene variant A/G snv 6.9E-02 2
rs2860580
HLA-A
1.000 0.120 6 29938914 upstream gene variant A/C;G;T snv 2
rs3129055 1.000 0.120 6 29702484 regulatory region variant A/G snv 0.24 2
rs9510787
TNFRSF19
1.000 0.120 13 23631056 intron variant A/G snv 0.20 2
rs2894207
LINC02571 ; HLA-B
0.882 0.160 6 31295974 intron variant T/C snv 0.20 7
rs1057519045
FGFR2
0.851 0.160 10 121498522 missense variant T/G snv 6
rs6774494
MECOM
0.882 0.160 3 169364845 intron variant G/A snv 0.42 2
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs180177133
PALB2
0.807 0.240 16 23614089 frameshift variant T/- delins 1.2E-05 1.4E-05 9
rs29232 0.925 0.240 6 29643654 intergenic variant C/T snv 0.39 3
rs3731239
CDKN2A
0.763 0.240 9 21974219 intron variant A/G snv 0.26 1
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 5
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25