Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs1129055
CD86
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 15
rs17281995
CD86
0.763 0.360 3 122120794 3 prime UTR variant G/A;C snv 11
rs375328708
STK11
1.000 0.120 19 1226602 synonymous variant C/G;T snv 6.7E-05 6.3E-05 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 127
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 117
rs2980874
TRIB1
0.925 0.120 8 125432546 intron variant G/A snv 0.30 2
rs2235108
TRIB1
0.925 0.120 8 125436547 3 prime UTR variant G/A snv 0.25 2
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 2
rs752967378
RAF1
0.882 0.160 3 12618580 missense variant G/A;C snv 4.0E-06 3
rs2066827
GPR19 ; CDKN1B
0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21
rs10094872
CASC11
0.882 0.200 8 127707639 intron variant A/T snv 0.33 1
rs1561927
LINC00824
0.807 0.280 8 128555832 intron variant C/T snv 0.65 5
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 73
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs35226131
TERT
1.000 0.120 5 1295258 upstream gene variant C/T snv 2.6E-02 1
rs141095230
MGMT
0.925 0.120 10 129536277 missense variant C/A;T snv 8.0E-06; 5.2E-05 2
rs12917
MGMT ; LOC105378560
0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs2308321
MGMT
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 6
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 36
rs488087
CEL
0.925 0.120 9 133071212 synonymous variant C/A;T snv 0.11 0.26 2
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 20
rs3124761
SLC2A6
0.925 0.120 9 133474633 intron variant T/C snv 0.80 2
rs9502893 0.827 0.120 6 1339954 intergenic variant C/G;T snv 3