Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs402710
CLPTM1L
0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38 18
rs4460498 0.925 0.120 9 97858130 downstream gene variant T/C snv 0.63 2
rs4752028
SHTN1
0.807 0.200 10 117075480 intron variant C/T snv 0.73 6
rs4791331
NTN1
0.925 0.120 17 9028765 intron variant C/T snv 0.53 3
rs522616
MMP3
0.763 0.320 11 102844317 upstream gene variant T/C snv 0.23 10
rs534391501
GRHL3
0.925 0.200 1 24334661 missense variant G/A snv 3.1E-04 1.7E-04 2
rs6072081
LOC102724968
0.851 0.120 20 40632414 intergenic variant A/G snv 0.49 4
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs7078160
SHTN1
0.851 0.120 10 117068049 intron variant G/A snv 0.19 4
rs7224837
AXIN2
0.925 0.200 17 65532005 intron variant G/A snv 0.89 2
rs7552506
IRF6
0.925 0.240 1 209796557 splice region variant G/C snv 0.32 0.32 2
rs757422353
CDH1
0.882 0.200 16 68823432 missense variant C/G snv 4.0E-06 3
rs770182236
NME1-NME2 ; NME1
0.925 0.200 17 51155707 missense variant G/A snv 6.4E-05 7.0E-06 2
rs772267475
NHLH1
1.000 0.120 1 160370811 missense variant G/A;C snv 8.6E-06 1
rs7850258
PTCSC2
0.827 0.200 9 97786731 intron variant A/G snv 0.72 6
rs8179096
TIMP2
0.851 0.200 17 78925567 upstream gene variant G/A;C snv 4
rs861019
IRF6
0.925 0.120 1 209802041 splice region variant A/G snv 0.44 2
rs876658146
CDH1
0.882 0.200 16 68815743 missense variant A/G snv 3