Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs116298963 1.000 0.080 6 32911694 intergenic variant A/G snv 1
rs116381494 1.000 0.080 6 28900717 downstream gene variant C/G snv 1
rs116442863 1.000 0.080 6 29122234 upstream gene variant G/A snv 1
rs116551911
DDR1
1.000 0.080 6 30896502 intron variant C/T snv 1
rs116668069 1.000 0.080 6 28800336 intergenic variant C/A;G snv 1
rs116718137 1.000 0.080 6 31228777 upstream gene variant T/C snv 1
rs116718336 1.000 0.080 6 33056722 regulatory region variant G/A snv 1
rs116826541 1.000 0.080 6 29180617 upstream gene variant A/G snv 1
rs11692700
LINC01829 ; LINC01828
1.000 0.080 2 67283245 intron variant T/C snv 2.2E-02 1
rs11780471 1.000 0.080 8 27487202 upstream gene variant G/A snv 4.3E-02 1
rs121909071
SLC22A18
1.000 0.080 11 2918030 missense variant C/T snv 7.0E-06 1
rs12201100
LOC105378031
1.000 0.080 6 141851652 intergenic variant A/G snv 4.7E-03 1
rs12439944
CSK
1.000 0.080 15 74783309 intron variant G/A;T snv 1
rs12964604 1.000 0.080 18 53635205 intergenic variant C/G;T snv 1
rs13199649 1.000 0.080 6 27901014 upstream gene variant C/T snv 5.0E-02 1
rs13201681
ZSCAN23
1.000 0.080 6 28426903 intergenic variant C/T snv 5.0E-02 1
rs13217620 1.000 0.080 6 27685341 upstream gene variant C/T snv 4.7E-02 1
rs1324578301
NTRK2
1.000 0.080 9 85020233 missense variant C/T snv 4.0E-06 1
rs139328189
TP53TG1
1.000 0.080 7 87332982 intron variant C/T snv 8.5E-03 1
rs1419255508
MXRA5
1.000 0.080 X 3310056 missense variant T/G snv 9.6E-06 1
rs144503462
LINC01347 ; SEPTIN14P21
1.000 0.080 1 243029970 intron variant T/C snv 2.8E-02 1
rs148791337
CROT
1.000 0.080 7 87356828 intron variant C/T snv 1.7E-02 1
rs151124926 1.000 0.080 2 67740157 intergenic variant A/G;T snv 1
rs1629083
MPZL2
1.000 0.080 11 118255861 intron variant C/T snv 0.50 1
rs17181550
LINC00511
1.000 0.080 17 72303817 intron variant T/G snv 0.38 1