Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 9
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 7
rs62033406
FTO
16 53790314 intron variant A/G snv 0.33 5
rs17001868
ADSL ; SGSM3 ; LOC107985538
0.925 0.080 22 40382227 intron variant A/C snv 0.12 3
rs17356907
PGAM1P5
0.925 0.080 12 95633983 intron variant A/G snv 0.28 3
rs6557160 6 151628447 intergenic variant A/C snv 0.35 2
rs9397437 1.000 0.080 6 151631197 intergenic variant G/A snv 6.6E-02 2
rs3205718
FAIM2
12 49868026 3 prime UTR variant C/T snv 0.30 2
rs34091558
LMOD1
1.000 0.040 1 201917642 intron variant A/- delins 0.25 2
rs616402
PEX14
1 10506215 intron variant C/T snv 0.29 2
rs10096213 8 36995695 regulatory region variant C/T snv 0.26 1
rs10110651 8 36989597 upstream gene variant T/C;G snv 1
rs12173570 6 151636579 intergenic variant C/T snv 0.21 1
rs12371778 12 28003148 intergenic variant C/A;G snv 1
rs146992477 8 36984537 downstream gene variant -/CTTTCTTTCT delins 0.25 1
rs17625845 2 120332155 intergenic variant T/C snv 0.15 1
rs1838564 12 28001962 intergenic variant G/A snv 8.1E-02 1
rs2359714 1 118227648 intergenic variant C/T snv 0.44 1
rs4820792 22 28765019 intergenic variant C/T snv 0.21 1
rs5752793 22 28764326 intergenic variant A/G snv 0.35 1
rs61280460 14 94329847 intergenic variant A/C;T snv 1
rs62105303 2 632922 intergenic variant G/A;T snv 1
rs6427508 1 160269067 intron variant T/C snv 0.63 1
rs7659874 4 74621799 regulatory region variant A/G snv 0.32 1