Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10494132
CHIA
0.851 0.080 1 111289601 upstream gene variant T/C snv 0.26 4
rs56317450
PHF14
1.000 0.080 7 11137720 intron variant G/A snv 0.18 1
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs143326447
MIR4435-2HG ; SOCAR
0.925 0.080 2 111511155 intron variant T/C snv 0.11 4
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs59289606
KIAA1958
1.000 0.080 9 112563085 intron variant C/A snv 0.16 1
rs2234678
IL1RN
0.925 0.080 2 113117988 5 prime UTR variant A/G snv 0.25 0.21 2
rs3814399
BOC
1.000 0.080 3 113272645 synonymous variant C/A;T snv 4.7E-04; 2.1E-02 1
rs1314595
ATRNL1
1.000 0.080 10 115148713 intron variant C/T snv 4.3E-02 1
rs892225
SBNO2
0.925 0.080 19 1152657 intron variant A/G snv 0.39 2
rs4807630
LOC102725180 ; SBNO2
1.000 0.080 19 1170446 intron variant C/T snv 0.26 1
rs980577637
NOS1
0.925 0.080 12 117265431 missense variant C/T snv 5.6E-05 2
rs76830467
NOS1
1.000 0.080 12 117321510 intron variant A/T snv 3.4E-02 2
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs2450083
COLEC10
1.000 0.080 8 119051303 intron variant T/C snv 0.59 2
rs928382 1.000 0.080 10 120122169 regulatory region variant C/G snv 0.99 1
rs1696361 0.925 0.080 12 120926020 TF binding site variant T/C snv 0.75 2
rs188074962 0.925 0.080 12 120927628 intergenic variant G/A snv 0.79 2
rs1806656
ILDR1
0.925 0.080 3 121997324 intron variant C/G snv 0.23 2
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs2069763
IL2
0.807 0.320 4 122456327 synonymous variant C/A snv 0.36 0.29 6
rs1716183
PITPNM2
1.000 0.080 12 123150549 upstream gene variant C/T snv 0.34 1
rs16929097 1.000 0.080 9 12521826 intergenic variant G/A snv 4.7E-02 1
rs8179521
MAP3K2-DT
1.000 0.080 2 127393348 intron variant A/C;G snv 1
rs1931704 1.000 0.080 10 127541545 intergenic variant G/A snv 0.28 1