Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 12
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
rs12459419
CD33
0.925 0.120 19 51225221 missense variant C/G;T snv 0.31 6
rs77960347
LIPG
18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03 6
rs3756668
PIK3R1
0.925 0.160 5 68300260 3 prime UTR variant G/A;C snv 5
rs4672497 2 62296430 TF binding site variant C/G;T snv 5
rs55709272
IL1RN
2 113109711 intron variant T/A;C snv 5
rs66505542
BUD13
11 116752498 intron variant AA/-;A;AAA delins 5
rs755249
PPIEL ; BMP8A
1 39529402 3 prime UTR variant C/A;T snv 5
rs9411378
ABO
9 133270015 intron variant A/C;T snv 5
rs11021221 11 95575690 intron variant T/A;G snv 4
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs144204502
TK1 ; AFMID
17 78187152 5 prime UTR variant C/G;T snv 1.2E-02 4