Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs4644
LGALS3
0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 12
rs498872
PHLDB1
0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 10
rs76151636
ATP7B
0.776 0.280 13 51944145 missense variant G/A;T snv 4.0E-06; 9.2E-04 10
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs1135401891
BRCA2
0.790 0.280 13 32332796 frameshift variant -/CT ins 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
rs753152604
CDK4
0.827 0.040 12 57751680 missense variant C/A snv 7
rs1373481065
GADD45A
0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
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
rs764803020
TP53
0.851 0.040 17 7673750 frameshift variant -/TTTCCGCCGG delins 4.0E-06 5
rs781490101
TP53
0.851 0.040 17 7673748 missense variant T/C snv 8.0E-06 5
rs865880036
MEIS2
0.827 0.040 15 37098156 missense variant A/C snv 1.3E-04 5
rs1029044314
DDR1
0.851 0.040 6 30898095 missense variant G/A snv 4
rs1320938886
BLZF1
0.851 0.040 1 169376605 missense variant T/G snv 4.0E-06 4
rs1340827343
TCF19 ; POU5F1
0.851 0.040 6 31165259 missense variant C/T snv 4
rs1381537616
HOXA10 ; HOXA9 ; HOXA10-HOXA9
0.851 0.040 7 27174132 missense variant C/T snv 4
rs28357681
ND6 ; CYTB
0.851 0.040 MT 14798 missense variant T/C snv 4
rs755794544
PDGFA
0.851 0.040 7 512435 missense variant T/C snv 4.0E-06 4
rs8057643
RBFOX1
0.851 0.040 16 6910689 intron variant C/A;T snv 4
rs374524467
PITX2
0.827 0.040 4 110632961 missense variant A/C snv 8.0E-06 7.0E-06 5