Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1086603 0.882 0.120 1 147816164 intergenic variant G/A snv 3.4E-02 3
rs16830359 1.000 0.080 1 43130713 intergenic variant G/A;T snv 3
rs16849542
ATF6
0.882 0.120 1 161816705 intron variant A/G snv 2.1E-02 3
rs6670122
MRPL24
0.882 0.120 1 156737983 intron variant T/C;G snv 0.99 3
rs11210604 0.925 0.080 1 42158001 downstream gene variant T/A;G snv 2
rs10915020 1.000 0.080 1 34692115 intergenic variant T/A snv 0.10 1
rs10918931 1.000 0.080 1 168592853 intergenic variant T/C snv 0.61 1
rs11165851
LOC105378867 ; DPYD
1.000 0.080 1 97380021 intron variant T/A snv 0.93 1
rs11206948
LOC105378745
1.000 0.080 1 56984813 intron variant T/C snv 3.6E-02 1
rs1163521 1.000 0.080 1 105786097 intergenic variant T/A;C;G snv 1
rs12123414 1.000 0.080 1 79919071 intergenic variant G/A;C snv 0.34 1
rs1395246
LOC105378771
1.000 0.080 1 63681491 intergenic variant G/C snv 1.8E-02 1
rs1496116 1.000 0.080 1 96687003 intergenic variant T/C snv 0.27 1
rs17131023
LRRC7
1.000 0.080 1 69753508 intron variant T/C snv 3.5E-02 1
rs17257155
CATSPER4
1.000 0.080 1 26199948 missense variant A/G snv 0.15 0.17 1
rs1749432
LINC01031
1.000 0.080 1 193322114 intron variant T/A snv 0.30 1
rs17586966
PSMA5
1.000 0.080 1 109412947 non coding transcript exon variant T/C snv 5.1E-02 1
rs1925335 1.000 0.080 1 196211214 intergenic variant A/G snv 0.98 1
rs2474121
DDAH1
1.000 0.080 1 85332355 intron variant G/A;C snv 1
rs2480408
SRGAP2
1.000 0.080 1 206450673 intron variant A/G snv 1.8E-02 1
rs2485570
RYR2
1.000 0.080 1 237122307 intron variant G/T snv 0.88 1
rs2861887
ASTN1
1.000 0.080 1 177072861 intron variant C/T snv 0.46 1
rs2997477
LOC105373108
1.000 0.080 1 224796665 intergenic variant G/C snv 0.77 1
rs3099627 1.000 0.080 1 11439331 intergenic variant A/G snv 0.98 1
rs348184
DAP3
1.000 0.080 1 155728019 intron variant A/G snv 6.7E-02 1