Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 14
rs1801320
RAD51 ; RAD51-AS1
0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 14
rs1057519902
H3-3A
0.742 0.160 1 226064451 missense variant G/C snv 13
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv 13
rs121909218
PTEN
0.672 0.360 10 87933145 missense variant G/A snv 12
rs3788266
S100B
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 12
rs11196067
VTI1A
0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs1205454520
KLLN ; PTEN
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06 10
rs2243248
IL4
0.763 0.240 5 132672952 upstream gene variant T/A;C;G snv 9
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81 9
rs4295627
CCDC26
0.763 0.200 8 129673211 intron variant T/G snv 0.17 9
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 8
rs3024994
VEGFA
0.776 0.120 6 43775770 non coding transcript exon variant C/T snv 3.8E-02 8
rs498872
PHLDB1
0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 8
rs12885300
DIO2 ; DIO2-AS1
0.790 0.200 14 80211923 5 prime UTR variant C/A;G;T snv 7
rs753152604
CDK4
0.827 0.040 12 57751680 missense variant C/A snv 7
rs1135401891
BRCA2
0.790 0.280 13 32332796 frameshift variant -/CT ins 6
rs1005230
VEGFA
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs11860248
RBBP6
0.882 0.040 16 24566445 intron variant T/G snv 0.27 5
rs149840192
EGFR
0.807 0.080 7 55154129 missense variant C/A;T snv 5
rs17296479 0.851 0.040 5 81411157 non coding transcript exon variant T/A snv 9.4E-02 5
rs17748
TREH ; PHLDB1
0.827 0.080 11 118657714 3 prime UTR variant C/T snv 0.18 5
rs2234248
LOC105375056 ; TREM2
0.827 0.040 6 41163980 upstream gene variant A/G snv 2.2E-03 5