Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1998081
CD93
20 23076845 upstream gene variant T/C snv 0.90 1
rs2144940 20 23070169 downstream gene variant C/G;T snv 1
rs2425051
FAM83C
20 35292560 upstream gene variant A/G;T snv 1
rs2567617 20 23068910 downstream gene variant G/A snv 0.88 1
rs6060288
PROCR ; MMP24-AS1-EDEM2
20 35184440 intron variant G/A snv 0.40 1
rs6083037 20 23201922 regulatory region variant A/T snv 0.15 1
rs6088618
NCOA6
20 34821547 5 prime UTR variant G/A;C;T snv 1
rs76223987
TRPC4AP
20 35030669 intron variant T/C snv 8.2E-02 1
rs77385328
ITCH
20 34457287 intron variant G/A snv 4.1E-02 1
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs1613662
GP6 ; LOC107985325
0.851 0.120 19 55025227 missense variant G/A snv 0.85 0.83 8
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs774723292
LDLR
1.000 0.080 19 11105249 missense variant C/T snv 2.8E-05 4
rs4805881
PEPD
19 33405526 intron variant A/C snv 0.69 3
rs12981279 19 10528857 intergenic variant T/C snv 0.41 1
rs143928955
DNM2
19 10732057 intron variant C/G snv 4.7E-02 1
rs1671135
NLRP2
19 55000505 intron variant G/C;T snv 1
rs4548995
SLC44A2
19 10630195 intron variant G/A;C snv 1
rs55724477
STX10 ; IER2
19 13152241 5 prime UTR variant C/G snv 0.40 1
rs7508633
STX10
19 13147476 intron variant A/G snv 0.40 1
rs28496996 18 1952126 intron variant T/G snv 3.1E-02 1
rs7245232 18 73992717 intron variant G/C snv 0.15 1
rs8089640
CCDC102B
18 69186114 intergenic variant C/T snv 9.2E-02 1
rs9945428
FBXO15
18 74121441 intron variant C/A snv 0.38 1
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 26