Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs712964 22 19168604 upstream gene variant T/C snv 0.66 2
rs8134546
LINC01426
1.000 0.080 21 34782568 intron variant T/C snv 8.7E-02 2
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 7
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs6506897 1.000 0.080 18 31215320 intergenic variant G/A snv 0.62 2
rs6506900
LOC105372049
1.000 0.080 18 31226433 intergenic variant A/C;G snv 2
rs10502575 18 31756628 downstream gene variant A/G snv 6.9E-02 1
rs616082 18 31787677 intergenic variant C/A;T snv 1
rs8089491 18 31763291 upstream gene variant G/A snv 5.4E-02 1
rs115689251
LOC107985068
1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs12051548
TM4SF5
17 4779740 intron variant G/C snv 7.5E-02 1
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 6
rs4788815
LOC105371334
16 71600908 intergenic variant A/T snv 0.69 3
rs10500569
LOC107984814
16 72722202 intron variant G/A;C;T snv 1
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs16939881
ALDH1A2 ; AQP9
15 58179780 intron variant G/C;T snv 2
rs6606859
GABRG3
1.000 0.080 15 27032254 intron variant C/A;T snv 2
rs77757620
STARD9
1.000 0.080 15 42661399 intron variant C/T snv 3.8E-02 2
rs2306786
MYO1E
15 59195731 intron variant C/G snv 8.0E-02 1
rs1303
SERPINA1
0.925 0.040 14 94378506 missense variant T/G snv 0.28 0.22 4
rs3809346
COL4A1 ; COL4A2
1.000 0.080 13 110308596 intron variant G/A;C snv 2
rs448792
FRY
1.000 0.080 13 32103287 intron variant T/A;C snv 2
rs543554
FRY
1.000 0.080 13 32127501 intron variant A/G;T snv 2