Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 56
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 13
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 21
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 20
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10 8
rs55832599
TP53
0.716 0.360 17 7673821 missense variant G/A snv 5
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 20
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs1555525012
TP53
0.882 0.200 17 7673603 missense variant G/A snv 2
rs17884306
TP53
0.925 0.120 17 7668783 3 prime UTR variant C/T snv 5.1E-02 2
rs2941471
HNF4G
0.851 0.240 8 75558169 intron variant G/A snv 0.65 2
rs2229629
HK2
0.882 0.120 2 74889400 missense variant G/A snv 6.0E-02 0.18 4
rs747601652
CRYZ
0.925 0.120 1 74723233 missense variant A/G snv 1.2E-05 2
rs9564966 0.851 0.120 13 73322084 intergenic variant A/G snv 0.52 4
rs11655237
LINC00511 ; LINC00673
0.724 0.280 17 72404025 non coding transcript exon variant C/T snv 0.16 17
rs1552462 0.925 0.120 11 7235910 upstream gene variant C/T snv 2.7E-02 2
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 36
rs149617956
MITF
0.672 0.560 3 69964940 missense variant G/A snv 1.4E-03 1.6E-03 20
rs1800566
NQO1
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1258159645
NQO1
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37