Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs747093473
CDX2
1.000 0.080 13 27968819 missense variant G/A snv 7.0E-06 1
rs2269772
ITGA3
0.925 0.080 17 50072022 synonymous variant C/T snv 0.17 0.19 6
rs11187842
PLCE1
0.925 0.080 10 94292754 intron variant C/T snv 7.8E-02 4
rs1305398818
ABCG2
0.925 0.080 4 88131886 missense variant G/A;C snv 4.0E-06; 4.0E-06 4
rs6087990
DNMT3B
0.925 0.080 20 32762102 upstream gene variant T/C;G snv 4
rs8193
CD44
0.925 0.080 11 35229771 3 prime UTR variant C/T snv 0.29 4
rs9589207
MIR17HG ; MIR92A1 ; MIR19B1 ; MIR20A ; MIR19A
0.925 0.080 13 91351335 mature miRNA variant G/A;C snv 5.4E-03; 4.0E-06 4
rs1064261
MTOR
0.925 0.080 1 11228701 missense variant G/A;T snv 0.75; 4.0E-06 3
rs111638916
PSMD10
0.925 0.080 X 108084839 3 prime UTR variant G/A snv 3
rs115785973
SOCS3
0.925 0.080 17 78357871 3 prime UTR variant C/G;T snv 3
rs12083239 0.925 0.080 1 39985357 intergenic variant G/A;C snv 3
rs12416605
MIR938 ; SVIL
0.925 0.080 10 29602331 mature miRNA variant C/T snv 0.22 0.20 3
rs154268
PRKAA1
0.925 0.080 5 40795766 intron variant C/T snv 0.69 3
rs17103265
NFKBIA
0.925 0.080 14 35405503 upstream gene variant A/- delins 3
rs199971565
MIR302A ; MIR302D ; MIR302CHG ; MIR302C ; LARP7 ; MIR367 ; MIR302B
0.925 0.080 4 112648384 mature miRNA variant ACTT/- delins 2.1E-02 3
rs2070803
TRIM46
0.925 0.080 1 155185239 intron variant G/A snv 0.55 3
rs2172362
LOC105378667
0.925 0.080 1 39829228 intergenic variant T/C snv 0.58 3
rs230310
TRIT1
0.925 0.080 1 39842047 intron variant A/G;T snv 3
rs3738708
PARP1
0.925 0.080 1 226402338 missense variant G/A;C snv 7.0E-06 3
rs377566281
XRCC1
0.925 0.080 19 43552083 missense variant C/T snv 5.6E-05 2.1E-05 3
rs461404
PRKAA1
0.925 0.080 5 40799438 upstream gene variant G/A snv 0.70 3
rs4635002
DOCK1
0.925 0.080 10 127064415 intron variant A/C snv 0.92 3
rs56288038
IRF1 ; IRF1-AS1
0.925 0.080 5 132483914 3 prime UTR variant G/C snv 2.0E-05 7.0E-06 3
rs5999749
MAPK1
0.925 0.080 22 21833371 intron variant A/C;T snv 3
rs759397296
CASP2
0.925 0.080 7 143294294 missense variant T/C snv 4.0E-06 3