Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs377566281
XRCC1
0.925 0.080 19 43552083 missense variant C/T snv 5.6E-05 2.1E-05 3
rs3781619
DDB2
0.882 0.080 11 47233766 intron variant G/A snv 0.26 3
rs3789210
PGC
0.882 0.080 6 41743584 intron variant C/G;T snv 3
rs3814896
TFF2 ; LOC105372815
0.882 0.080 21 42351602 upstream gene variant A/G snv 0.17 3
rs4460629 0.882 0.080 1 155162859 intergenic variant T/C snv 0.56 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
rs4646421
CYP1A1
0.882 0.080 15 74723851 intron variant G/A;C;T snv 0.21 3
rs4711690
PGC
0.882 0.080 6 41741200 missense variant C/G snv 0.19 0.20 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
rs6939861
MIR10398 ; TFEB
0.882 0.080 6 41735303 intron variant G/A snv 0.24 3
rs753724
PLCE1
0.882 0.080 10 94291660 intron variant G/A;C;T snv 3
rs759397296
CASP2
0.925 0.080 7 143294294 missense variant T/C snv 4.0E-06 3
rs7853122
RAPGEF1
0.925 0.080 9 131705224 intron variant C/T snv 0.87 3
rs804270
NEIL2
0.882 0.080 8 11770112 5 prime UTR variant G/C;T snv 3
rs9981660 0.882 0.080 21 42317828 upstream gene variant G/A snv 0.11 3
rs10022537
PROM1
0.925 0.080 4 16075214 intron variant A/T snv 0.70 2
rs10052016
SLC6A3
0.925 0.080 5 1427996 intron variant A/G snv 0.22 2
rs10088390
SFRP1
0.925 0.080 8 41264249 3 prime UTR variant C/G snv 0.19 2
rs1011445550
TP53
0.925 0.080 17 7676391 missense variant G/C snv 2
rs10421916
INSL3
0.925 0.080 19 17818178 intron variant A/G snv 0.69 2
rs1044432
BTBD10
0.925 0.080 11 13388251 3 prime UTR variant A/T snv 0.16 2
rs10464867
OSGIN2 ; NBN
0.925 0.080 8 89933370 3 prime UTR variant C/T snv 3.0E-02 2
rs10474606
THBS4
0.925 0.080 5 80057163 intron variant G/A snv 0.28 2