Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs11119805
LPGAT1
1 211744902 3 prime UTR variant T/A snv 0.13 2
rs11120822
CAMTA1
1 7053052 intron variant G/C snv 0.34 2
rs16838623
CHRM3
1 239648090 intron variant A/C snv 3.4E-02 2
rs2391388
ALG14
1 95020269 intron variant A/C snv 0.49 2
rs6671200
TLCD4-RWDD3 ; LOC101928118
1 95231973 intron variant A/C snv 0.90 2
rs6675668
ALG14
1 95050081 intron variant T/G snv 0.43 2
rs860873
CNN3
1 94921652 intron variant G/A snv 0.39 2
rs16850871
GALNT2
1 230083723 intron variant A/G snv 0.11 1
rs6683451
LINC01036 ; ERVMER61-1
1 187323476 intron variant A/C snv 7.1E-02 1
rs7513659
GALNT2
1 230090639 intron variant G/A snv 8.5E-02 1
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs13431652
SPC25
0.925 0.080 2 168896905 intron variant T/C snv 0.24 5
rs12623456 2 163162632 intergenic variant T/C snv 2.2E-02 2
rs2118674
MYO3B
2 170462384 intron variant A/T snv 0.87 2
rs6722456 2 133771520 intergenic variant G/A snv 4.5E-02 2
rs77164426 2 146756888 intergenic variant A/G snv 1.8E-02 2
rs11695051
LOC107985897 ; SFXN5
2 73007303 intron variant T/C snv 5.2E-02 1
rs34440628
LOC105373898 ; LOC105373899
2 221659167 intergenic variant G/A;C snv 1
rs334809
IL5RA
0.925 0.080 3 3088537 intron variant A/G;T snv 4
rs1913185
LOC105374145
3 146170670 intergenic variant T/G snv 0.15 2
rs2581624 3 142915027 intron variant G/C;T snv 0.29 2
rs7611820
SLC7A14-AS1
3 170654068 non coding transcript exon variant G/A snv 0.22 1
rs10518201
LOC101928893
4 78730706 regulatory region variant A/G snv 6.2E-02 1
rs10518202 4 78758523 intergenic variant G/T snv 9.6E-02 1