Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 5
rs12355840
MIR202 ; MIR202HG
0.827 0.240 10 133247608 non coding transcript exon variant C/G;T snv 1.1E-04; 0.80 5
rs1884302 0.851 0.120 20 7125642 intron variant T/C snv 0.41 4
rs7501477 0.851 0.160 17 78930194 upstream gene variant G/A;T snv 4
rs3114018
ABCG2
0.882 0.160 4 88143429 intron variant A/C snv 0.48 4
rs10851907
CHRNB4
1.000 0.040 15 78623522 upstream gene variant G/A snv 0.40 4
rs2287074
MMP2
0.851 0.120 16 55493201 synonymous variant G/A;C snv 0.39; 8.0E-06 4
rs1784418
MMP20 ; LOC101928477
0.851 0.080 11 102613665 intron variant C/A;T snv 0.41 4
rs8054556
TMEM219
0.925 0.080 16 29946895 intron variant G/A;C;T snv 4
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 3
rs6441989 0.882 0.120 3 46433408 downstream gene variant A/G snv 0.53 3
rs3737665
CA6
0.925 0.080 1 8970905 missense variant C/G;T snv 4.0E-06; 0.26 3
rs1800971
DEFB1
0.882 0.120 8 6870594 3 prime UTR variant T/C snv 8.0E-02 3
rs3796704
ENAM
0.882 0.120 4 70643714 missense variant G/A snv 7.0E-02 0.13 3
rs2232387
KRT75
1.000 0.040 12 52433824 missense variant C/T snv 0.13 0.14 3
rs2232398
KRT75
0.925 0.120 12 52430567 missense variant C/T snv 7.4E-03 6.5E-03 3
rs35874116
TAS1R2
1.000 0.040 1 18854899 missense variant T/C snv 0.29 0.31 3
rs17074565 0.925 0.080 13 81668577 intergenic variant C/G snv 0.12 2
rs5933871
AMELX ; ARHGAP6
0.925 0.080 X 11295537 intron variant T/C snv 0.33 2
rs761996476
AMELX ; ARHGAP6
0.925 0.080 X 11298573 missense variant T/C snv 5.5E-06 2
rs5934997
ARHGAP6 ; AMELX
0.925 0.080 X 11295613 intron variant T/C snv 0.33 2
rs10864376
CA6
0.925 0.080 1 8970313 intron variant C/A;T snv 2
rs12138897
CA6
0.925 0.080 1 8971844 intron variant C/A;G;T snv 2
rs17032907
CA6
0.925 0.040 1 8950346 intron variant C/T snv 0.17 2
rs2274328
CA6
0.925 0.040 1 8949385 missense variant A/C snv 0.49 0.51 2