Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs150400940
LOC105378486 ; LOC107984268
10 112050671 intergenic variant C/T snv 3.0E-02 2
rs76124550
VTI1A
10 112626980 intron variant C/T snv 2.2E-02 2
rs114780919
GRAMD1C
3 113931599 intron variant C/T snv 4.5E-02 2
rs142034933 5 114906794 intergenic variant T/A;G snv 2
rs145880548 6 115097886 intergenic variant A/G snv 1.9E-02 2
rs55922880 12 115179836 intergenic variant T/C snv 3.6E-02 2
rs1003858
PAPPA
9 116202676 intron variant G/C snv 1.1E-02 2
rs187568415 19 11623811 downstream gene variant G/A snv 4.8E-02 2
rs9924009
TXNDC11
16 11688193 intron variant G/A;T snv 2
rs114167782
LOC105375467 ; CFTR ; WNT2
7 117299233 intron variant C/T snv 3.0E-02 2
rs137949660
KSR2
12 117495695 intron variant G/C snv 2.0E-02 2
rs144850704
KSR2
12 117624269 intron variant C/T snv 6.7E-02 2
rs189087047
LOC105375721
8 117639150 intergenic variant C/T snv 1.6E-02 2
rs12731372 1 118310352 regulatory region variant C/T snv 0.19 3
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs12143789
TBX15
1 118954531 intron variant G/C snv 0.13 2
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs1106529
TBX15
1 118988874 intron variant G/A snv 0.77 3
rs2645294
WARS2
1 119031964 3 prime UTR variant C/T snv 0.59 4
rs5957117
KIAA1210
X 119130439 intron variant C/T snv 6.6E-02 2
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs113991851 4 12025243 intergenic variant C/T snv 2.1E-02 2
rs80261602
CADPS2
7 122631261 intron variant C/G snv 1.3E-02 2
rs116383923
SNX29
16 12381345 intron variant C/G snv 2
rs12317176
CCDC92 ; DNAH10
12 123920171 intron variant T/C snv 0.39 3