Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs877610
TRPV1
1.000 17 3572196 synonymous variant C/T snv 4.6E-02 7.5E-02 3
rs1800876
CMA1
1.000 14 24510007 upstream gene variant G/A snv 0.24 2
rs7201637
HSD17B2
1.000 16 82081670 intron variant T/A snv 9.0E-02 2
rs775040765
BRAF
1.000 7 140800366 missense variant T/C snv 8.0E-05 1.4E-05 2
rs1405999227
EGFR
0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 3
rs2640
EIF2AK1
0.925 0.080 7 6026819 missense variant T/C snv 9.0E-02 5.5E-02 3
rs391745 0.925 0.080 X 97839482 intergenic variant C/G;T snv 3
rs471979
NLRP5
0.925 0.080 19 56027610 missense variant G/C snv 0.13 9.7E-02 3
rs58124832
CACNA1H
0.925 0.080 16 1218376 missense variant G/A;T snv 5.5E-02 3
rs6162
CYP17A1
0.925 0.080 10 102837224 synonymous variant G/A snv 0.42 0.40 3
rs61731956
NR1H3 ; MADD
0.925 0.080 11 47268596 missense variant G/A snv 2.2E-04 2.6E-04 3
rs483352809
TUBB4A
0.882 0.120 19 6495754 missense variant C/T snv 5
rs1062577
ESR1
0.882 0.080 6 152102770 3 prime UTR variant T/A;G snv 4
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs121912456
SOD1 ; LOC102724449
0.851 0.120 21 31659806 missense variant G/C snv 6
rs774994509
SOD1
0.851 0.080 21 31667296 missense variant A/G snv 4.0E-06 5
rs121908585
PDGFRA
0.827 0.080 4 54285926 missense variant A/T snv 9
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8
rs121912433
SOD1
0.827 0.120 21 31663841 missense variant G/A snv 4.0E-06 7
rs121912436
SOD1
0.827 0.080 21 31667274 missense variant G/A;C snv 7
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs28937900
FKRP
0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 37
rs74315409
PRNP
0.742 0.240 20 4699915 missense variant T/G snv 6.0E-05 2.1E-05 13
rs1800875
CMA1
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41 12