Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 12
rs4295627
CCDC26
0.763 0.200 8 129673211 intron variant T/G snv 0.17 11
rs6971
TSPO
0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs76151636
ATP7B
0.776 0.280 13 51944145 missense variant G/A;T snv 4.0E-06; 9.2E-04 10
rs1205454520
KLLN ; PTEN
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06 10
rs498872
PHLDB1
0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 10
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81 10
rs371409680
TP53
0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 10
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs2904551
PRODH
0.776 0.160 22 18918421 missense variant A/G snv 5.2E-03 2.8E-03 8
rs3024994
VEGFA
0.776 0.120 6 43775770 non coding transcript exon variant C/T snv 3.8E-02 8
rs1135401891
BRCA2
0.790 0.280 13 32332796 frameshift variant -/CT ins 7
rs753152604
CDK4
0.827 0.040 12 57751680 missense variant C/A snv 7
rs12885300
DIO2 ; DIO2-AS1
0.790 0.200 14 80211923 5 prime UTR variant C/A;G;T snv 7
rs149840192
EGFR
0.807 0.080 7 55154129 missense variant C/A;T snv 7
rs769809364
TP73
0.807 0.080 1 3732940 missense variant G/A snv 8.5E-06 1.4E-05 7
rs1453633223
CDKN2A
0.807 0.080 9 21974503 missense variant C/T snv 4.0E-06 6
rs63750949
FBXO11 ; MSH6
0.827 0.080 2 47806213 missense variant C/A;T snv 6
rs1373481065
GADD45A
0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs660118
SART1
0.807 0.080 11 65967703 missense variant G/C snv 0.46 0.36 6
rs745542298
TP73
0.807 0.080 1 3732781 missense variant G/A;T snv 8.6E-06; 4.3E-06 2.1E-05 6
rs17296479 0.851 0.040 5 81411157 non coding transcript exon variant T/A snv 9.4E-02 5
rs2440472
AMFR
0.827 0.080 16 56402912 intron variant A/G snv 0.61 5
rs373191257
AMFR
0.827 0.080 16 56363027 missense variant T/A snv 1.6E-05 7.0E-06 5
rs3092993
ATM ; C11orf65
0.827 0.040 11 108364388 intron variant C/A snv 0.11 5