Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs1784418
MMP20 ; LOC101928477
0.851 0.080 11 102613665 intron variant C/A;T snv 0.41 4
rs1884302 0.851 0.120 20 7125642 intron variant T/C snv 0.41 4
rs3114018
ABCG2
0.882 0.160 4 88143429 intron variant A/C snv 0.48 4
rs8054556
TMEM219
0.925 0.080 16 29946895 intron variant G/A;C;T snv 4
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
rs12640848
ENAM
0.925 0.080 4 70640695 intron variant A/G snv 0.47 2
rs149467613
P2RY2
1.000 0.040 11 73232438 intron variant G/A snv 3.3E-02 2
rs17032907
CA6
0.925 0.040 1 8950346 intron variant C/T snv 0.17 2
rs2735733
MUC5B
1.000 0.040 11 1240410 intron variant C/T snv 0.49 0.43 2
rs2857476
MUC5B
1.000 0.040 11 1259904 intron variant T/C snv 0.54 2
rs478927
MMP13
0.925 0.080 11 102954097 intron variant T/C snv 0.68 2
rs5933871
AMELX ; ARHGAP6
0.925 0.080 X 11295537 intron variant T/C snv 0.33 2
rs5934997
ARHGAP6 ; AMELX
0.925 0.080 X 11295613 intron variant T/C snv 0.33 2
rs931608
ZNF98
1.000 0.040 19 22431320 intron variant A/C;T snv 2
rs10180496 1.000 0.040 2 12828774 intron variant A/G snv 0.15 1
rs10242311
ATXN7L1
1.000 0.040 7 105633273 intron variant A/C snv 6.2E-02 1
rs10987008
PBX3
1.000 0.040 9 125899321 intron variant T/A snv 0.54 1
rs1122171
C5orf66
1.000 0.040 5 135174297 intron variant C/T snv 0.56 1
rs11672900
MAMSTR
1.000 0.040 19 48717066 intron variant A/G;T snv 1
rs12602978 1.000 0.040 17 27240054 intron variant C/T snv 9.3E-02 1
rs1383934
ADAMTS3
1.000 0.040 4 72551807 intron variant G/A snv 0.68 1
rs140357883
MTMR3
1.000 0.040 22 29896823 intron variant T/-;TT;TTT delins 1