Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 21
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 11
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 10
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 9
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 6
rs13219787
H2AC17 ; H2BC17
6 27893892 upstream gene variant G/A;T snv 3.9E-02; 2.4E-04 5
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv 5
rs2794719
LOC108783645 ; HFE
0.925 0.120 6 26088662 intron variant T/C;G snv 5
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs55709272
IL1RN
2 113109711 intron variant T/A;C snv 5
rs5756504
TMPRSS6
22 37071230 intron variant C/G;T snv 5
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5
rs9379818 0.925 0.120 6 26022978 downstream gene variant G/A;T snv 5
rs9804550 11 5164863 intergenic variant T/A;C snv 5
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4
rs11756659 6 25933704 upstream gene variant A/G;T snv 4