Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17001868
ADSL ; SGSM3 ; LOC107985538
0.925 0.080 22 40382227 intron variant A/C snv 0.12 2
rs2229712
RPS6KA1
0.925 0.080 1 26557020 missense variant A/C snv 0.22 0.17 2
rs345299
VAV3
0.925 0.080 1 107905511 intron variant A/C snv 0.69 2
rs3734805
CCDC170 ; LOC107986528
0.925 0.080 6 151618215 3 prime UTR variant A/C snv 6.9E-02 2
rs3736729
GCLC
0.925 0.080 6 53514607 intron variant A/C snv 0.44 2
rs374486449
MSH6 ; FBXO11
0.925 0.080 2 47798814 missense variant A/C snv 2.0E-05 5.6E-05 2
rs431825416
BRCA1
0.925 0.080 17 43051093 missense variant A/C snv 2
rs56156320
FSCN1
0.925 0.080 7 5592480 upstream gene variant A/C snv 0.49 2
rs57890595
TNFRSF10D
0.925 0.080 8 23146600 intron variant A/C snv 0.16 2
rs5956583
XIAP
0.925 0.080 X 123900661 missense variant A/C snv 0.33 0.39 2
rs62382272
MIR378A ; PPARGC1B
0.925 0.080 5 149731403 intron variant A/C snv 0.14 2
rs650490
PDE10A
0.925 0.080 6 165491803 intron variant A/C snv 0.29 2
rs7027604
ALDH1A1
0.925 0.080 9 72940036 intron variant A/C snv 0.46 2
rs7329797
RCBTB1
0.925 0.080 13 49572410 intron variant A/C snv 3.1E-02 2
rs777214281
RECQL
0.925 0.080 12 21486512 missense variant A/C snv 1.8E-04 1.3E-04 2
rs9693444 0.925 0.080 8 29652100 intergenic variant A/C snv 0.66 2
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 41
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs28366003
MT2A
0.763 0.240 16 56608579 upstream gene variant A/C;G snv 4.6E-02 10
rs1997623
CAV1
0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 9
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 8
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 8
rs1800264
DMD
0.827 0.120 X 32699141 missense variant A/C;G snv 5.5E-06; 8.3E-03 5